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Recalls in November 2019

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    Stacked Gourd Jack-O-Lantern decorations recalled

    The string light wiring inside the Jack-O-Lanterns can overheat

    Mark Feldstein & Associates of Sylvania, Ohio, is recalling about 5,000 Stacked Gourd Jack-O-Lantern decorations.

    The string light wiring inside the Jack-O-Lanterns can overheat, spark or ignite, posing a fire hazard.

    The firm has received four reports of the Jack-O-Lantern decorations smoking or catching fire. No injuries or property damage are reported.

    This recall involves Stacked Gourd Jack-O-Lantern decorations. The 12-inch Jack-O-Lantern is hand-painted resin and has battery-operated LED string lights inside the product.

    The Jack-O-Lantern’s lights are powered with three AAA batteries. Printed on a hang tag and a label on the box is UPC code 789683062481, model number S1915D12 and Mark Feldstein & Associates Inc.

    The decorations, manufactured in China, were sold at Paper Store, Hallmark stores, and independent gift stores nationwide from August 2019, through October 2019, and online at www.Amazon.com from July 2019, through September 2019, for about $20.

    What to do

    Consumers should immediately stop using the recalled Stacked Gourd Jack-O-Lantern decorations and contact Mark Feldstein & Associates to receive a full refund.

    Consumers may contact Mark Feldstein & Associates at (800) 755-6504 from 8:15 a.m. to 5 p.m. (ET) Monday through Friday, by email at Sales@MFAgifts.com or online at www.MFAgifts.com and click on “Recall Information” at the top of the page for more information.

    Mark Feldstein & Associates of Sylvania, Ohio, is recalling about 5,000 Stacked Gourd Jack-O-Lantern decorations.The string light wiring inside the Jac...
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    Golden State Medical Supply recalls Ranitidine Hydrochloride capsules

    The product may contain N-Nitrosodimethylamine above levels established by the FDA.

    Golden State Medical Supply (GSMS) is recalling all quantities and lots of Ranitidine HCl 150-mg and 300-mg capsules.

    The product may contain N-Nitrosodimethylamine (NDMA ), a substance that could cause cancer, above levels established by the FDA.

    The firm has not received any reports of adverse events.

    The following products, used for treatment of gastric disorders, are being recalled:

    Product DescriptionGSMS NDCGSMS Lot #Expiration Date
    RANITIDINE HCl 150MG CAPSULES 500 Ct Bottle51407-097-05GS02397010/31/2020
    GS02610810/31/2020
    GS02609910/31/2020
    GS02683810/31/2020
    GS02570210/31/2020
    GS02727210/31/2020
    GS02727305/31/2021
    RANITIDINE HCl 300MG CAPSULES 100 Ct Bottle51407-098-01GS02397110/31/2020
    GS02552710/31/2020
    GS02552610/31/2020
    GS02611410/31/2020
    GS02581310/31/2020
    GS02618910/31/2020
    GS02755507/31/2021
    GS02619005/31/2021
    GS02622005/31/2021
    GS02658405/31/2021
    GS02713905/31/2021
    GS02755405/31/2021

    The lots being recalled were primarily sold to AmerisourceBergen, McKesson, and Tricare Mail Order Pharmacies (TMOP).

    What to do

    Patients taking the recalled products should consult with their physician, pharmacist, or healthcare provider about an alternative treatment prior to discontinuing the use of the medication.

    Once an alternative treatment has been prescribed, patients should contact the recall processor at (866) 382-8606 or by email at Novitiumpharma6639@stericycle.com to obtain instructions and kit for returning the remaining product.

    Consumers with questions may contact GSMS at (800) 284-8633, ext. 215 Monday through Friday from 7:30 AM to 4:00 PM (PT) by fax at (805) 437-7588 or by email at recalls@gsms.us

    Golden State Medical Supply (GSMS) is recalling all quantities and lots of Ranitidine HCl 150-mg and 300-mg capsules.The product may contain N-Nitrosod...
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      CHS recalls Payback Feeds

      The products may contain high levels of magnesium

      CHS of Inver Grove Heights, Minn., is recalling 67 tons of Payback Feeds.

      The products may contain high levels of magnesium.

      Excess dietary magnesium in animals could result in osmotic diarrhea and a marked decrease in feed intake and result in death.

      The company has received reports of the deaths of 403 pheasants.

      The following products, bagged in 50 lb. bags that display the Payback Feed brand, are being recalled:

      Product NameLot NumberManufacture Date
      Payback Champion RabbitM644310 09/30/2019
      Payback Egg Layer Ration PelletM644570 09/30/2019
      Payback Egg Layer Ration KrumbleM644550 09/30/2019
      Payback Turkey /Pheasant Grower A MedicatedM650210 10/04/2019
      Payback Turkey /Pheasant GrowerM644560 09/30/2019
      Payback Swine Complete BreederM643210 09/27/2019
      Payback Waterfowl FeedM644540 09/30/2019

      The recalled products were distributed in Wyoming and Montana from September 9 – October 4, 2019.

      What to do

      Customers who purchased the recalled products should immediately stop using and return them to their local dealer or directly to CHS for full refund.

      If animals that consumed the recalled products have the above symptoms, a veterinarian should be contacted.

      Consumers with questions may contact the from at (406) 453-7646 from 8 a.m. – 4 p.m. (MST) Monday – Friday.

      CHS of Inver Grove Heights, Minn., is recalling 67 tons of Payback Feeds.The products may contain high levels of magnesium.Excess dietary magnesium...
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      Voyager Industries recalls Yetti Fish House Angler, Grand Excape and Traxx trailers

      The wheel may come off the axle assembly, posing a crash risk

      Voyager Industries is recalling 1,062 model year 2018-2020 Yetti Fish House Angler, Grand Excape and Traxx trailers.

      The vehicles may be missing retainer clips at the spindle nut, potentially causing the spindle nut to loosen and fall off.

      If the spindle nut loosens or falls off, the wheel may come off the axle assembly, posing the risk of a crash.

      What to do

      Voyager Industries will notify owners, and, if missing, dealers will install retainer clips at the spindle nut free of charge.

      The recall began November 11, 2019.

      Owners may contact Voyager Industries customer service at (800) 834-4940.

      Voyager Industries is recalling 1,062 model year 2018-2020 Yetti Fish House Angler, Grand Excape and Traxx trailers.The vehicles may be missing retaine...
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      Nature’s Rx recalls Silver Bullet male enhancement

      The product contains sildenafil, which is not declared on the label

      Nature’s Rx is recalling one lot of Silver Bullet, which is marketed as a male enhancement.

      An FDA laboratory analysis found the product to contain sildenafil, a PDE-5 inhibitor not declared on the label that may pose serious health risks to consumers with underlying medical issues.

      The firm has not received any reports of adverse events.

      The recalled product is contained in blister foil sheets and packaged in small boxes containing 10 capsules with an expiration date of November 2022, and lot number: 01251ZX1.

      It was sold on online.

      What to do

      Nature’s Rx is notifying its customers by replacement or refund and is arranging for return or replacement of all recalled products. Customers who purchased the recalled product should stop using it and discard or return it.

      Consumers with questions may contact Nature’s Rx at (888) 925-5551 Monday – Friday from 10 AM – 6 PM (PST). By email at naturesrxsales@gmail.com, or by mail at 310 N Indian Hill Blvd Ste 600, Claremont, CA 91711

      Nature’s Rx is recalling one lot of Silver Bullet, which is marketed as a male enhancement.An FDA laboratory analysis found the product to contain sild...
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      SCARPA North America recalls ski boots

      The ski boot shell can crack, posing a fall hazard

      SCARPA North America of Boulder, Colo., is recalling about 5,400 Maestrale RS and Maestrale Men’s ski boots sold in the U.S., and Canada.

      The ski boot shell can crack, posing a fall hazard and risk of injury to the consumer.

      This recall involves the Fall 2017 Maestrale RS and Maestrale Men’s Ski Boots.

      The Maestrale style numbers are #12047/501.1 and can be identified by their orange color, and the “SCARPA” name on lower-outside shell and “Maestrale” model name on upper/outside cuff.

      The Maestrale RS style numbers are #12046/501.1 and can be identified by their white, black and lime color, and the “SCARPA” name on lower-outside shell and “Maestrale RS” model name on upper/outside cuff.

      UPC_

      EAN

      Style

      Number

      Descrip.

      Vendor

      SKU

      Color

      Size2

      666898

      700837

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-24.5

      White/

      Black/

      Lime

      24.5

      666898

      700844

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-25.0

      White/

      Black/

      Lime

      25

      666898

      700851

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-25.5

      White

      /Black/

      Lime

      25.5

      666898

      700868

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-26.0

      White/

      Black/

      Lime

      26

      666898

      700875

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-26.5

      White

      /Black

      /Lime

      26.5

      666898

      700882

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-27.0

      White

      /Black

      /Lime

      27

      666898

      700899

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-27.5

      White/

      Black/

      Lime

      27.5

      666898

      700905

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-28.0

      White

      /Black

      /Lime

      28

      666898

      700912

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-28.5

      White

      /Black

      /Lime

      28.5

      666898

      700929

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-29.0

      White/

      Black

      /Lime

      29

      666898

      700936

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-29.5

      White/

      Black/

      Lime

      29.5

      666898

      700943

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-30.0

      White

      /Black

      /Lime

      30

      6668987

      00950

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-30.5

      White/

      Black/

      Lime

      30.5

      666898

      700967

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-31.0

      White

      /Black/

      Lime

      31

      666898

      700974

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-31.5

      White/

      Black/

      Lime

      31.5

      666898

      700981

      12046/

      501.1

      MAEST-

      RALE RS (F17)

      12046/501.1-WhtBlkLim-32.0

      White/

      Black

      /Lime

      32

      666898

      700455

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-24.5

      Orange

      24.5

      666898

      700462

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-25.0

      Orange

      25

      666898

      700479

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-25.5

      Orange

      25.5

      666898

      700486

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-26.0

      Orange

      26

      666898

      700493

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-26.5

      Orange

      26.5

      666898

      700509

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-27.0

      Orange

      27

      666898

      700516

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-27.5

      Orange

      27.5

      666898

      700523

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-28.0

      Orange

      28

      666898

      700530

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-28.5

      Orange

      28.5

      666898

      700547

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-29.0

      Orange

      29

      666898

      700554

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-29.5

      Orange

      29.5

      666898

      700561

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-30.0

      Orange

      30

      666898

      700578

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-30.5

      Orange

      30.5

      666898

      700585

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-31.0

      Orange

      31

      666898

      700592

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-31.5

      Orange

      31.5

      666898

      700608

      12047/

      501.1

      MAEST-

      RALE RS (F17)

      12047/501.1-Orng-32.0

      Orange

      32

      The boots, manufactured in Italy, were sold at authorized SCARPA dealers and outdoor stores nationwide and online at www.scarpa.com from August 2017, through August 2019, for $700 for the Maestrale model and $800 for the Maestrale RS model.

      What to do

      Consumers should immediately stop using the recalled ski boots and contact SCARPA for instructions on returning the boot to receive a free boot shell repair. SCARPA is contacting all known purchasers directly.

      Consumers may contact SCARPA toll-free at (866) 998-2895 from 8 a.m. to 5 p.m. (MT) Monday through Friday, by email at recall@scarpa.com, or online at www.scarpa.com and click on “Fall 2017 Maestrale RS and Maestrale Ski Boot Recall” at the top of the page for more information.

      SCARPA North America of Boulder, Colo., is recalling about 5,400 Maestrale RS and Maestrale Men’s ski boots sold in the U.S., and Canada.The ski boot s...
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      Mazda recalls CX-7, CX-9 and Mazda6 vehicles

      The passenger front airbag inflators may explode

      Mazda North American Operations is recalling 69,879 model year 2007-2012 CX-7, CX-9 and model year 2009-2012 Mazda6 vehicles.

      The vehicles had their passenger front airbag inflators previously replaced under a prior recall using inflators of the same design.

      The inflators may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, temperature and temperature cycling.

      An inflator explosion may result in sharp metal fragments striking the driver or other occupants resulting in serious injury or death.

      What to do

      Mazda will notify owners, and dealers will replace the front passenger air bag inflator with an alternate one free of charge.

      The recall is expected to begin December 18, 2019.

      Owners may contact Mazda customer service at (800) 222-5500, option 4. Mazda's number for this recall is 1317F.

      Mazda North American Operations is recalling 69,879 model year 2007-2012 CX-7, CX-9 and model year 2009-2012 Mazda6 vehicles.The vehicles had their pas...
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      Natural Grocers recalls organic soybeans

      The product may contain mold

      Vitamin Cottage Natural Food Market of Lakewood, Colo., is recalling Natural Grocers brand organic soybeans.

      The product may contain mold.

      The following product, packaged in clear plastic bags weighing two pounds and bearing the “Natural Grocers” label and the packed-on dates 19-168 and 19-205, are being recalled:

      UPC CodeDescriptionPacked on Dates
      000080663607Organic Soybeans 2 LB19-168 & 19-205

      The packed-on date can be found in the bottom left-hand corner of the label.

      The recalled product was shipped to 154 Natural Grocers’ stores located in Arkansas, Arizona, Colorado, Iowa, Idaho, Kansas, Louisiana, Minnesota, Missouri, Montana, Nebraska, Nevada, New Mexico, North Dakota, Oklahoma, Oregon, Texas, Utah, Washington and Wyoming.

      Specific locations of those stores may be found here

      What to do

      Customers who purchased the recalled product should discontinue use and discard or return it to the store for credit or refund.

      Consumers with questions may contact the company at (303) 986-4600, ext. 80801, Monday through Friday 8:00 a.m. to 5:00 p.m. (MST).

      Vitamin Cottage Natural Food Market of Lakewood, Colo., is recalling Natural Grocers brand organic soybeans.The product may contain mold.The follow...
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      Forest River recalls model year 2020 Surveyor trailers,

      The 12V refrigerator has a fuse with incorrect amperage

      Forest River is recalling 19 model year 2020 Surveyor trailers, model SVT33KFKDS.

      A fuse with incorrect amperage was installed for the 12V refrigerator, potentially allowing the wiring to overheat.

      If the wiring overheats, an electrical short can occur, increasing the risk of a fire.

      What to do

      Forest River has notified owners, and dealers will replace the incorrect fuse with one of the correct amperage free of charge.

      The recall began November 7, 2019.

      Owners may contact Forest River customer service at (260) 499-2100. Forest River's number for this recall is 37-1108.

      Forest River is recalling 19 model year 2020 Surveyor trailers, model SVT33KFKDS.A fuse with incorrect amperage was installed for the 12V refrigerator,...
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      Grace Digital recalls EcoBoulder speakers

      The speaker’s battery can become overcharged and burst

      Grace Digital of San Diego, Calif., is recalling about 88,000

      ECOXGEAR EcoBoulder speakers.

      The speaker’s battery can become overcharged and burst, posing an impact hazard.

      ECOXGEAR has received five reports of speaker batteries bursting and fragmenting, including two incidents of property damage to the surrounding area. No injuries have been reported.

      This recall involves the ECOXGEAR EcoBoulder Bluetooth Speakers., which is black in color with a rubber slip mat on top and about 20” tall and 15” wide.

      There are four versions which have a color accent around the front speaker and a matching rubber slip mat. There is a storage compartment located on the left side of the speaker.

      The model number GDI-EXBM900 series is labeled on the inside door of the speaker’s storage compartment.

      ECOXGEAR is printed on the front of the speakers.

      Model Number

      UPC Code

      GDI-EXBM900 (Orange)

      819127010331

      GDI-EXBM901 (Black)

      819127010348

      GDI-EXBM904 (Yellow)

      819127011796

      GDI-EXBM907 (Red)

      819127011802

      GDI-EXBM913  (Blue)

      819127011819

      The speakers, manufactured in China, were sold at Costco stores nationwide from October 2016, to January 2017, at Academy Sports, Cabela’s, Home Depot and Best Buy stores nationwide and online at Amazon.com from January 2018, through December 2018, for about $180.

      What to do

      Consumers should immediately stop using the recalled speakers and contact ECOXGEAR to receive a free battery replacement kit.

      Consumers may contact ECOXGEAR at (800) 903-9664 from 8 a.m. to 8 p.m. (CT) Monday through Friday, by email at safety@ecoxgear.com, or online at www.ecoxgear.com and click on "SAFETY ALERT" for EcoBoulder at the top of the page header or at www.ecoxgear.com/safetynotice for more information.

      Grace Digital of San Diego, Calif., is recalling about 88,000ECOXGEAR EcoBoulder speakers.The speaker’s battery can become overcharged and burst, p...
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      Keystone recalls model year 2019-2020 Crossroads Sunset trailers

      The interior range cooktop burner flame may invert, posing a fire risk

      Keystone RV Company is recalling 157 model year 2019-2020 Crossroads Sunset trailers, model 242BH.

      The interior range cooktop is installed in a cabinet that may not be entirely sealed from the furnace cavity. As a result, during furnace operation, the interior range cooktop burner flame may invert.

      If the cooktop burner flames invert, there is an increased risk of a fire and injury.

      What to do

      Keystone will notify owners, and dealers will inspect the interior range cooktop with the furnace running, sealing it as necessary, free of charge.

      The recall is expected to begin December 16, 2019.

      Owners may contact Keystone customer service at (866) 425-4369. Keystone's number for this recall is 19-362.

      Keystone RV Company is recalling 157 model year 2019-2020 Crossroads Sunset trailers, model 242BH.The interior range cooktop is installed in a cabinet...
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      Deck Source recalls Cutek Proclean

      The product is labeled improperly

      Deck Source of Canada is recalling about 1,850 containers of Cutek Proclean Professional Wood Restoration sold in the U.S., and Canada.

      The product contains the hazardous substance oxalic acid. The product label violates the Federal Hazardous Substance Act by omitting the word “poison” and printing the mandatory hazard statement for poisonous chemicals on the back of the label instead of the front, posing a risk of poisoning if swallowed by children.

      No incidents or injuries are reported.

      This recall involves Cutek Proclean Professional Wood Restoration, sold in a clear plastic one-gallon bottle with a blue, black and white label.

      “Cutek Proclean Professional Wood Restoration” is printed on the front of the product and UPC 098411800166 is printed on the side panel of the product.

      The wood restoration product, manufactured in Australia, was sold at DK Sales, Meteek Supply, Alpine Lumber, Thermory USA, Niece Lumber, Shipshe Sealers and Gable Lumber from May 2014, through October 2019, for about $65.

      What to do

      Consumers should immediately stop using the recalled product, move it out of the reach of children and contact Deck Source for a free replacement label to put on the product.

      Consumers may contact Deck Source toll-free at (844) 442-8835 from 9 a.m. to 4 p.m. (ET) Monday through Friday, by email at sales@cutekstain.com or online at www.cutekstain.com and click on “Contact Us” at the top of the page for more information.

      Deck Source of Canada is recalling about 1,850 containers of Cutek Proclean Professional Wood Restoration sold in the U.S., and Canada.The product cont...
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      B&B Acquisition recalls Wintergreen Essential Oils

      The packaging of the product is not child resistant

      B&B Acquisition of Salt Lake City, Utah, is recalling about 67,700 packages of Airome Wintergreen Essential Oil and Deep Soothe Essential Oil 100 percent Pure & Natural Therapeutic Grade Essential Oils.

      The product contains the substance methyl salicylate, which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA).

      The packaging of the product is not child resistant, posing a poisoning risk if the contents are swallowed by young children.

      No incidents or injuries are reported.

      This recall involves Airome Wintergreen 100% pure essential oils in 0.5- and 0.34-fluid-ounce amber glass dropper bottles sold without a child-resistant cap.

      It also includes Airome Deep Soothe 100% pure essential oils in 0.5-fluid-ounce amber glass dropper bottles sold without a child-resistant cap.

      Each bottle has a black cap and blue label with either “Airome Wintergreen 100% Pure Essential Oil Stimulate” or “Airome Deep Soothe 100% Pure Essential Oil Cool” printed on the front. A UPC code unique to each type of recalled bottle –83324503131, 833245034567, or 833245035977 – is printed on the bottom of the gift box in which the bottles were sold.

      The Arome Wintergreen 100% Pure Essential Oil Stimulate was sold separately and as part of a 3-pack “Focus & Concentrate Essential Oil Gift Set.”

      The oils, manufactured in the U.S., were sold at home specialty stores and gift shops nationwide and online at Amazon.com from December 2016, through July 2019, for between $12 and $20.

      What to do

      Consumers should immediately store the product in a safe location out of the reach of children and contact B&B Acquisition for a free replacement child-resistant cap.

      Consumers may contact B&B Acquisition at (800) 262-2305 from 8 a.m. to 5 p.m. (MT) Monday through Friday or by email at info@airome.com.

      B&B; Acquisition of Salt Lake City, Utah, is recalling about 67,700 packages of Airome Wintergreen Essential Oil and Deep Soothe Essential Oil 100 percent...
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      United National Closeout Stores recalls isometric exercise devices

      The handle grips on each end can break during use

      United National Closeout Stores (UNCS) of Fort Lauderdale, Fla., is recalling about 1,500 ISO7X isometric exercise devices.

      The handle grips on each end can break during use and cause parts to be ejected forcefully from the shaft, posing a risk of injury from impact to the user or bystander.

      The firm has received 10 reports of the handles breaking and the ejection of the internal spring coil and rod, including five reports of impact injuries that resulted in punctures and lacerations.

      This recall involves Ontel ISO7X isometric exercise devices.

      The device is about three feet long with hard plastic black handle grips on each end and two black nylon straps that extend down opposite sides of the center metal shaft.

      Only isometric exercise devices with black handle grips are involved.

      The exercise devices, manufactured in China, were sold at Burlington Stores nationwide from January 2019, through March 2019, for about $7.

      What to do

      Consumers should immediately stop using the recalled device and contact UNCS to receive instructions on how to obtain a full refund.

      Consumers may contact UNCS collect at (954) 524-3325 from 8 a.m. to 5 p.m. (ET) Monday through Friday or by email at email help@uncs.com.

      United National Closeout Stores (UNCS) of Fort Lauderdale, Fla., is recalling about 1,500 ISO7X isometric exercise devices.The handle grips on each end...
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      Forest River recalls East to West Delta Terra and Silver Lake recreational trailers

      The overhead bunk fasteners may not be secured properly

      Forest River is recalling 27 model year 2020 East to West Delta Terra (model 312BH) and East to West Silver Lake (model 31KBH) recreational trailers.

      The overhead bunk fasteners may not be properly secured to the backer board of the bunk.

      As a result, the bunk may fall, posing an injury risk.

      What to do

      Forest River has notified owners, and dealers will secure the bunk to the backer properly free of charge.

      The recall began November 1, 2019.

      Owners may contact Forest River customer service at (574) 264-6664. Forest River's number for this recall is 500-1112.

      Forest River is recalling 27 model year 2020 East to West Delta Terra (model 312BH) and East to West Silver Lake (model 31KBH) recreational trailers.Th...
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      Kettle Cuisine recalls Marketside Creamy Cauliflower Parmesan Soup

      The product may contain fish and wheat, allergens not declared on the label

      Kettle Cuisine of Lynn, Mass., is recalling Marketside Brand Creamy Cauliflower Parmesan Soup.

      The product may contain fish and wheat, allergens not declared on the label.

      No adverse reactions or illnesses have been reported to date.

      The recalled product is packed into 16-oz plastic retail lidded cups labeled as ‘Marketside Brand Creamy Cauliflower Parmesan Soup’ with UPC 8113130636 and use-by dates ranging from 11/23/19 to 01/01/20 inclusive.

      It was distributed to Walmart stores in all 50 states for purchase in store or online.

      What to do

      Customers who purchased the recalled product should dispose of it or return it to the store where purchased for a refund.

      Consumers with may contact Kettle Cuisine at (617) 409-1290 between 9AM and 5PM EST, Monday through Friday.

      Kettle Cuisine of Lynn, Mass., is recalling Marketside Brand Creamy Cauliflower Parmesan Soup.The product may contain fish and wheat, allergens not dec...
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      TMC recalls Chateau, Daybreak, Four Winds, Freedom Elite Quantum motorhomes

      The seatbelt-unfastened warning light is slow to illuminatewill not illuminat

      Thor Motor Coach (TMC) is recalling 378 model year 2019-2020 Chateau 22B, 22E, 23U, 24F, 25V, & 28A, Daybreak 22GO, Four Winds 22B, 22E, 24F, 26B & 28A, Freedom Elite 22HE, and 2020 Quantum GR22 & SE22 motorhomes.

      The seatbelt-unfastened warning light will not illuminate for approximately five seconds after the ignition is moved to the "on" or "start" position.

      Without the seatbelt warning reminder, the driver may forget to fasten the seatbelt, increasing the risk of injury in a crash.

      What to do

      TMC owners will be notified, and dealers will reprogram the instrument panel cluster free of charge.

      The recall began October 3, 2019.

      Owners may contact Chevrolet customer service at (800) 630-2438, GMC customer service at (800) 462-8782 or TMC customer service at (877) 855-2867. TMC's number for this recall is RC000177.

      Thor Motor Coach (TMC) is recalling 378 model year 2019-2020 Chateau 22B, 22E, 23U, 24F, 25V, & 28A, Daybreak 22GO, Four Winds 22B, 22E, 24F, 26B & 28A, Fr...
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      Amneal Pharmaceuticals recalls Ranitidine tablets and syrup

      The medications are contaminated with a probable cancer-causer

      Amneal Pharmaceuticals of Bridgewater, N.J., is recalling Ranitidine tablets and syrup.

      The products are contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

      The products are used for multiple indications, including treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.

      There are no reports of adverse events.

      Products with the following lot numbers are being recalled:

      Ranitidine Tablets, USP, 150 mg

      Description

      Lot#

      Expiration Date

      Ranitidine Tablets, USP 150mg

      AR180483B

      3/31/2020

      Ranitidine Tablets, USP 150mg

      AR180559A

      3/31/2020

      Ranitidine Tablets, USP 150mg

      AR180560A

      3/31/2020

      Ranitidine Tablets, USP 150mg

      AR180594A

      3/31/2020

      Ranitidine Tablets, USP 150mg

      AR180595A

      3/31/2020

      Ranitidine Tablets, USP 150mg

      AR180675A

      4/30/2020

      Ranitidine Tablets, USP 150mg

      AR180829A

      4/30/2020

      Ranitidine Tablets, USP 150mg

      AR180831A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180832A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180868A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180868B

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180869A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180870A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180871A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180872A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180995A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180996A

      5/31/2020

      Ranitidine Tablets, USP 150mg

      AR180997A

      6/30/2020

      Ranitidine Tablets, USP 150mg

      AR180998A

      6/30/2020

      Ranitidine Tablets, USP 150mg

      AR181158A

      7/31/2020

      Ranitidine Tablets, USP 150mg

      AR181159A

      7/31/2020

      Ranitidine Tablets, USP 150mg

      AR181160A

      7/31/2020

      Ranitidine Tablets, USP 150mg

      AR181161A

      7/31/2020

      Ranitidine Tablets, USP 150mg

      AR181690A

      10/31/2020

      Ranitidine Tablets, USP 150mg

      AR181691A

      10/31/2020

      Ranitidine Tablets, USP 150mg

      AR181692A

      10/31/2020

      Ranitidine Tablets, USP 150mg

      AR181693A

      10/31/2020

      Ranitidine Tablets, USP 150mg

      AR181694A

      10/31/2020

      Ranitidine Tablets, USP 150mg

      AR181709A

      10/31/2020

      Ranitidine Tablets, USP 150mg

      AR181710A

      11/30/2020

      Ranitidine Tablets, USP 150mg

      AR181711A

      11/30/2020

      Ranitidine Tablets, USP 150mg

      AR181806A

      11/30/2020

      Ranitidine Tablets, USP 150mg

      AR181807B

      11/30/2020

      Ranitidine Tablets, USP 150mg

      AR181807C

      11/30/2020

      Ranitidine Tablets, USP 150mg

      AR181808A

      11/30/2020

      Ranitidine Tablets, USP 150mg

      AR190004A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190005A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190006A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190007A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190008A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190008B

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190085A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190086A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190087A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190088A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190089A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190090A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190121A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190122A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190123A

      12/31/2020

      Ranitidine Tablets, USP 150mg

      AR190124A

      1/31/2021

      Ranitidine Tablets, USP 150mg

      AR190125B

      1/31/2021

      Ranitidine Tablets, USP 150mg

      AR190181A

      1/31/2021

      Ranitidine Tablets, USP 150mg

      AR190182A

      1/31/2021

      Ranitidine Tablets, USP 150mg

      AR190183A

      1/31/2021

      Ranitidine Tablets, USP 150mg

      AR190184A

      1/31/2021

      Ranitidine Tablets, USP 150mg

      AR190364A

      2/28/2021

      Ranitidine Tablets, USP 150mg

      AR190365A

      2/28/2021

      Ranitidine Tablets, USP 150mg

      AR190366A

      2/28/2021

      Ranitidine Tablets, USP 150mg

      AR190366B

      2/28/2021

      Ranitidine Tablets, USP 150mg

      AR190509A

      3/31/2021

      Ranitidine Tablets, USP 150mg

      AR190510A

      3/31/2021

      Ranitidine Tablets, USP 150mg

      AR190542B

      3/31/2021

      Ranitidine Tablets, USP 150mg

      AR190609A

      3/31/2021

      Ranitidine Tablets, USP 150mg

      AR190610A

      3/31/2021

      Ranitidine Tablets, USP 150mg

      HD03119A

      3/31/2021

      Ranitidine Tablets, USP 150mg

      HD03219A

      3/31/2021

      Ranitidine Tablets, USP 150mg

      HE03119A

      4/30/2021

      Ranitidine Tablets, USP 150mg

      HE03219A

      4/30/2021

      Ranitidine Tablets, USP, 300 mg

      Description

      Lot#

      Expiration Date

      Ranitidine Tablets, USP 300mg

      AR180519A

      3/31/2020

      Ranitidine Tablets, USP 300mg

      AR180613A

      3/31/2020

      Ranitidine Tablets, USP 300mg

      AR180615A

      3/31/2020

      Ranitidine Tablets, USP 300mg

      AR180638A

      3/31/2020

      Ranitidine Tablets, USP 300mg

      AR180640A

      4/30/2020

      Ranitidine Tablets, USP 300mg

      AR180641A

      4/30/2020

      Ranitidine Tablets, USP 300mg

      AR181156A

      7/31/2020

      Ranitidine Tablets, USP 300mg

      AR181157A

      7/31/2020

      Ranitidine Tablets, USP 300mg

      AR181795A

      11/30/2020

      Ranitidine Tablets, USP 300mg

      AR181920A

      12/31/2020

      Ranitidine Tablets, USP 300mg

      AR181921A

      12/31/2020

      Ranitidine Tablets, USP 300mg

      AR181921B

      12/31/2020

      Ranitidine Tablets, USP 300mg

      AR190414B

      2/28/2021

      Ranitidine Tablets, USP 300mg

      AR190415A

      2/28/2021

      Ranitidine Tablets, USP 300mg

      AR190416A

      2/28/2021

      Ranitidine Tablets, USP 300mg

      AR190417A

      2/28/2021

      Ranitidine Tablets, USP 300mg

      AR190418A

      2/28/2021

      Ranitidine Tablets, USP 300mg

      AR190418B

      2/28/2021

      Ranitidine Tablets, USP 300mg

      AR190543A

      3/31/2021

      Ranitidine Tablets, USP 300mg

      AR190544A

      3/31/2021

      Ranitidine Tablets, USP 300mg

      AR190545A

      3/31/2021

      Ranitidine Tablets, USP 300mg

      AR190705A

      4/30/2021

      Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL

      Description

      Lot#

      Expiration Date

      Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL

      06648001A

      11/2019

      Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL

      06648003A

      04/2020

      Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL

      06649001A

      01/2021

      The Ranitidine tablets and syrup being recalled can be identified by the following NDC numbers, which are on the product label:

      Product

      Strength

      Pack Size

      NDC Number

      Ranitidine Tablets, USP150 mg60 count65162-253-06
      Ranitidine Tablets, USP150 mg100 count65162-253-10
      Ranitidine Tablets, USP150 mg180 count65162-253-18
      Ranitidine Tablets, USP150 mg500 count65162-253-50
      Ranitidine Tablets, USP150 mg1000 count65162-253-11
      Ranitidine Tablets, USP300 mg30 count65162-254-03
      Ranitidine Tablets, USP300 mg100 count65162-254-10
      Ranitidine Tablets, USP300 mg250 count65162-254-25
      Ranitidine Tablets, USP300 mg1000 count65162-254-11
      Ranitidine Tablets, USP150 mg500 count53746-253-05
      Ranitidine Tablets, USP150 mg1000 count53746-253-10
      Ranitidine Syrup (Ranitidine Oral Solution, USP)15 mg/mL; 16 fl. oz.473 mL65162-664-90

      What to do

      Patients who have experienced any problems that may be related to the use of this recalled product. should contact their physician or healthcare provider

      Consumers who have the recalled products should stop using them and can call Stericycle at (866) 918-8768, Monday – Friday, 8:00 am – 5:00 pm (EST) for further information.

      Amneal Pharmaceuticals of Bridgewater, N.J., is recalling Ranitidine tablets and syrup.The products are contaminated with N-Nitrosodimethylamine (NDMA)...
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      Flying Tiger Copenhagen recalls crocodile candleholders

      The candleholders are flammable and can catch fire

      Flying Tiger of Copenhagen, Denmark, is recalling about 180 crocodile candleholders.

      The candleholders are flammable and can catch fire, posing a fire hazard when the candle burns down.

      The company has received one report of the candleholder catching fire. No injuries have been reported.

      This recall involves Flying Tiger Copenhagen candleholders shaped as a gold-colored crocodile. The candleholders measure 7 inches long by 2 inches wide. The candle holder is inside the crocodile’s wide open mouth.

      A hangtag attached to the holder reads, “Lysestage – Candle holder” and on the back “Item # 3017653, Batch # 218377”

      The candleholders, manufactured in China, were sold at Flying Tiger Copenhagen stores nationwide from September 2019, through October 2019, for about $4.

      What to do

      Consumer should immediately stop using the recalled candleholders and contact Flying Tiger for a full refund.

      Consumers may contact Flying Tiger Copenhagen toll-free at (844) 350-0560 from 8 a.m. to 5 p.m. (ET) Monday through Friday, by email at info.us@flyingtiger.com or online at www.flyingtiger.com and click on “Product Information” at the bottom of the page more information.

      Flying Tiger of Copenhagen, Denmark, is recalling about 180 crocodile candleholders.The candleholders are flammable and can catch fire, posing a fire h...
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      Med Man Recalls Up2

      The dietary supplement contains sildenafil rendering it an unapproved drug

      Med Man Distribution is recalling all lots of Up2 dietary supplement.

      The product, marketed as an “all-natural libido for men and women,” is tainted with sildenafil, making it an unapproved drug for which safety and efficacy have not been established.

      The firm says it has not received any reports of adverse events.

      Lots of the recalled product include 240 ten-count units, UPC 85606300322, 480 four-count packages, UPC 856063006315, and 960 singlepack units, UPC856063006308.

      It was sold in the U.S. to Regal Labs and their retailers.

      What to do

      Med Man is notifying its distributors and their customers by email and is arranging for destruction of all recalled products.

      Customers who purchased the recalled product should stop using and return it to the place of purchase for a refund.

      Consumers with questions may contact Med Man at (705) 297-5321 Monday – Friday, 9 am – 5pm (ET) or by email at dirtyderek669@gmail.com.

      Med Man Distribution is recalling all lots of Up2 dietary supplement.The product, marketed as an “all-natural libido for men and women,” is tainted wit...
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      You Chang Trading recalls Tilapia filets

      The product was not inspected upon being imported into the U.S.

      You Chang Trading of Brooklyn, N.Y., is recalling an undetermined amount of raw Tilapia filets.

      The product was not inspected upon being imported into the U.S.

      There are no confirmed reports of adverse reactions.

      The following frozen, raw item, produced between November 13, 2018, and January 5, 2019, is being recalled:

      • 22-lb. white cardboard boxes containing “CONWAY TILAPIA FILLETS PRODUCT OF HONGKONG” and lot codes 20181113, 20181203, or 20190105 and sell by dates of 11/16/2020, 12/03/2020, or 01/05/2021 represented on the label.

      The recalled product was shipped to distributor and retail locations in Massachusetts, New Jersey, New York and Pennsylvania.

      What to do

      Customers who purchased the recalled product should not consume it but discard or return it to the place of purchase.

      Consumers with questions may contact Yang Zhou Lu at (718) 633-7816.

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      Quest Products recalls ALOCANE Emergency Burn Pads

      The packaging is not child resistant as required by law

      Quest Products of Pleasant Prairie, Wis., is recalling 153,000 packages of ALOCANE Emergency Burn Pads.

      The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pads contain lidocaine, posing a risk of poisoning to young children if they were to place the pad in their mouth.

      No incidents or injuries are reported.

      This recall involves ALOCANE Emergency Burn Pads (10-count and 15-count) which come in a white and red box with “MAXIMUM STRENGTH ALOCANE Emergency Burn Pads” printed on the front.

      The product is an over the counter Gel Infused Pad with lidocaine (4%) as the active ingredient the lot numbers 4179, 4180, 4235, 4645, 4646 or 4698 printed next to the barcode on the box.

      The UPC number for the affected product is 8-46241-02448-7 and is located on the bottom of the box.

      The pads, manufactured in the U.S., were sold at Walgreens, Walmart, Target, Kroger, Meijer, other pharmacies nationwide, and online at Amazon.com, HomeDepot.com, Overstock.com, MyQuestStore.com and Alocane.com from March 2018, through June 2019, for about $9.

      What to do

      Consumers should immediately stop using the recalled burn pads, store them in a safe location out of reach of children and contact Quest Products to return the pain relieving pads for a free ALOCANE Emergency Burn Gel 2.5 ounce child resistant tube or a full refund.

      Consumers may contact Quest Products at (800) 650-0113 from 9 a.m. to 5 p.m. (CT) Monday through Friday, or online at www.alocane.com and click on “Contact Us” at the bottom of the page for more information.

      Quest Products of Pleasant Prairie, Wis., is recalling 153,000 packages of ALOCANE Emergency Burn Pads.The packaging is not child resistant as required...
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      Forest River recalls Dynamax DX3 and Force motorhomes

      The front axle stabilizer bracket may break

      Forest River is recalling 14 model year 2017 Dynamax DX3 and Force motorhomes.

      The front axle stabilizer bracket may not properly mount to the axle, and may break as a result.

      If the stabilizer bracket breaks, a sudden loss of vehicle control could occur, increasing the risk of a crash.

      What to do

      Forest River has notified owners, and a Detroit Diesel dealer will perform the recall remedy.

      The stabilizer brackets and I-beams will be inspected and spacers and replacement stabilizer brackets will be installed, as necessary, free of charge.

      The recall began November 6, 2019.

      Owners may contact Forest River customer service at (800) 348-7440 or find a Detroit Diesel location at www.detroitdiesel.com/locations/default.aspx.

      Forest River's number for this recall is 55-1105.

      Forest River is recalling 14 model year 2017 Dynamax DX3 and Force motorhomes.The front axle stabilizer bracket may not properly mount to the axle, and...
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      H&H Sports recalls VCAN V531 motorcycle helmets

      The helmet may separate from the wearer's head in a crash

      H&H Sports Protection is recalling 4,218 VCAN V531 motorcycle helmets in sizes XS, S, M, L, XL, and XXL, sold exclusively through Amazon.

      The helmet retention system may fail, allowing the helmet to separate from the wearer's head in a crash.

      A helmet that doesn't stay secured to the head can increase the risk of injury.

      What to do

      Amazon will notify the helmet purchasers and instruct them to return the helmets for a full refund.

      The recall is expected to begin in November 2019.

      Owners may contact H&H Sports at (626) 444-0107.

      H&H; Sports Protection is recalling 4,218 VCAN V531 motorcycle helmets in sizes XS, S, M, L, XL, and XXL, sold exclusively through Amazon.The helmet re...
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      Mystery Ranch recalls semi-automatic handgun holsters

      The retention strap can disconnect from the holster, allowing the handgun to fall

      Mystery Ranch of Bozeman, Mont., is recalling about 500 Quick Draw Side Arm Holster – Semi-Auto.

      The retention strap can disconnect from the holster and allow the handgun to fall. If this this happens, the gun can unexpectedly discharge, posing a serious injury risk.

      The firm has received 42 reports of the strap disconnecting from the holster, including one report of the gun unexpectedly coming out of a holster. No injuries have been reported.

      This recall involves the Mystery Ranch Quick Draw Side Arm Holster – Semi-Auto holsters designed to be used with semi-automatic firearms.

      The holsters have a camel hypalon exterior, foam cushioning and a snap closure.

      Mystery Ranch; Date on Tracking Tag: 28 May, 2019; Bundle No.: 294411; Line: S-B and Inspection: M-V are printed on the tracking tag inside of the recalled holster. UPC number 888564163139 is printed on the packaging.

      The holsters, manufactured in the Philippines, were sold at Al’s Sporting Goods, Archery Country, Bering’s, Bink’s Outfitters, Bull Basin Archery, Capital Sports, Farwest Sports, Gardenswartz Sporting Goods Archery, Pappas Trading Post, Rusted Moon Outfitters, Scheels, Shedhorn Sports, Trail Head Montana, and Wind River Outdoor Company nationwide and online at Al’s Sporting Goods, Archery Country, Bering’s, goHUNT.com, Mountain Archery, MysteryRanch.com, Scheels, Schnee’s, Shedhorn Sports, and TacticalGear.com from August 2019, through October 2019, for about $25.

      What to do

      Consumers should immediately stop using the recalled holsters and contact Mystery Ranch for a full refund. The firm is contacting all known purchasers directly.

      Consumers may contact Mystery Ranch toll-free at (833) 548-1999 from 9 a.m. to 5 p.m. (MT) Monday through Friday, by e-mail at customerservice@mysteryranch.com or online at www.mysteryranch.com and click on “Product Recalls” at the bottom of the page for more information

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      Forest River recalls EVO, Salem and Wildwood travel trailers

      The cooktops were installed with an improper liquid propane gas line

      Forest River is recalling 41 model year 2020 EVO, Salem and Wildwood travel trailers.

      The trailer cooktops were installed with a rubber liquid propane (LP) gas line instead of a copper one.

      The rubber hose may melt, allowing gas to enter the vehicle, increasing the risk of a fire.

      What to do

      Forest River has notified owners, and dealers will replace the rubber LP gas line with a copper gas line free of charge.

      The recall began November 7, 2019.

      Owners may contact Forest River customer service at (909) 873-3777. Forest River's number for this recall is 67A-1107.

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      Mill Stream Corp. recalls Cold Smoked Salmon

      The product may be contaminated with Clostridium botulinum

      Mill Stream Corp. (Sullivan Harbor Farm) of Hancock, Maine, is recalling ten lots of Cold Smoked Salmon.

      The product may be contaminated with Clostridium botulinum, which can cause life-threatening illness or death.

      No illnesses have been reported to date.

      The recalled product, sold between March 6, 2019, and September 17, 2019, in vacuum sealed packages in the following sizes: whole salmon side, 2 lb., 1 lb., 8 oz., and 4 oz., is marked with the following lot numbers marked on the back of the packages: 7049, 7050, 7051, 7052, 7054, 7056, 7058, 7060, 7062, 7066.

      It was sold and distributed through retail, wholesale and online orders in Maine, Massachusetts, Vermont, Rhode Island, New York, Connecticut, Pennsylvania, New Jersey, Ohio, Utah, Iowa, Tennessee, Minnesota, Colorado, Florida, Arizona, Wisconsin, Washington, Georgia, Illinois, Virginia, Michigan and Texas.

      What to do

      Customers who purchased the product should not use the product even if it does not look or smell spoiled, but discard it immediately.

      Consumers with questions may contact the company at (207) 266-0621 Monday – Friday, 8am – 5pm (EST).

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      Keystone recalls model year 2020 Dutchmen Atlas trailers

      The trailer may have an improper propane supply hose

      Keystone RV Company is recalling five model year 2020 Dutchmen Atlas 3382BH trailers.

      The trailers may have a non-metallic propane supply hose installed inside the burner box of the cooktop, instead of a copper supply hose.

      Under certain conditions, the heat from the range burner may cause the hose to melt and leak propane, increasing the risk of a fire or an injury.

      What to do

      Keystone will notify owners, and dealers will remove the non-metallic propane gas line and attach it to a copper propane gas line free of charge.

      The recall is expected to begin November 15, 2019.

      Owners may contact Keystone customer service at (866) 425-4369. Keystone's number for this recall is 19-363.

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      Jayco recalls model year 2017 Pinnacle Fifth Wheel trailers

      The suspension system may fail

      Jayco is recalling 908 model year 2017 Pinnacle Fifth Wheel trailers.

      The vehicle's suspension may allow the tires to contact the structure when under a certain load, which can cause damage to the tires.

      If the tire becomes damaged, causing premature tire wear, it can cause loss of vehicle control and increase the risk of a crash.

      What to do

      Jayco will notify owners, and dealers will inspect the condition of the leaf spring, rubber equalizer and bump stop clearance, and provide replacement of the leave spring or rubber equalizer if necessary. This repair will be done free of charge.

      The recall is expected to begin December 2, 2019.

      Owners may contact Jayco customer service at (800) 517-9137. Jayco's number for this recall is 9901443.

      Jayco is recalling 908 model year 2017 Pinnacle Fifth Wheel trailers.The vehicle's suspension may allow the tires to contact the structure when under a...
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      Airstream recalls model year 2019-2020 Atlas motorhomes

      Some of the 12V circuits may have insufficient overcurrent protection

      Airstream is recalling 151 model year 2019-2020 Atlas motorhomes.

      The SH1 Breaker Terminal may be wired incorrectly, causing some of the 12V circuits to have insufficient overcurrent protection.

      Incorrectly fused wires may overheat, increasing the risk of a fire.

      What to do

      Airstream will notify owners, and dealers will correct the wiring, as necessary, free of charge.

      The recall is expected to begin December 14, 2019.

      Owners may contact Airstream customer service at (877) 596-6505 or (937) 596-6111, extension 7401 or 7411.

      Airstream is recalling 151 model year 2019-2020 Atlas motorhomes.The SH1 Breaker Terminal may be wired incorrectly, causing some of the 12V circuits to...
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      Padrino Foods recalls beef tamales

      The products are labeled as beef and sirloin tamales but contain pork

      Padrino Foods of Irving, Texas, is recalling approximately 1,931 pounds of beef tamales.

      Although the products are labeled as beef and sirloin tamales, they actually contain pork.

      There are no confirmed reports of adverse reactions.

      The following fully-cooked, not shelf-stable items, produced on May 8, 2019, are being recalled:

      • 60-oz. packages containing “padrino foods BEEF & SIRLOIN TAMALES Homestyle in corn husks” with lot code 2128903 and a sell-by date 12-27-19.

      The recall products, bearing establishment number “EST. 13136” inside the USDA mark of inspection, were sold at retail locations in Kansas, Louisiana, Oklahoma and Texas.

      What to do

      Customers who purchased the recalled products should not consume them, but discard or return them to the place of purchase.

      Consumers with questions may contact Diane Luther at (214) 905-3444.

      Padrino Foods of Irving, Texas, is recalling approximately 1,931 pounds of beef tamales.Although the products are labeled as beef and sirloin tamales,...
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      Skylight recalls power adapters

      The casing can break when plugged into an electrical outlet

      Skylight of San Francisco, Calif., is recalling about 65,000 Series I power adapters for Skylight digital photo frames sold in the U.S., and Canada.

      The power adapter casing can break when plugged into an electrical outlet, exposing its metal prongs, posing an electrical shock hazard.

      The firm has received eight reports of adapters breaking and exposing its metal prongs, including one report of an electric shock to a consumer.

      This recall involves the Series I power adapters sold with Skylight digital photo frames. The power adapters are black and have a circular indentation on the side. UPC code 679113611535 can be found on the packaging.

      Only the Series I adapters are included in this recall.

      The adapters, manufactured in China, were sold online at www.skylightframe.com and Amazon.com, and in Von Maur stores nationwide from April 2018, through March 2019, for about $160 with the digital photo frame.

      What to do

      Consumers should immediately stop using the recalled adapters and contact Skylight for instructions on proper disposal and how to receive a free replacement adapter. Skylight is contacting all known purchasers directly.

      Consumers may contact Skylight toll-free at (888) 359-4389 from 8 a.m. to 7 p.m. (ET) Monday through Friday, by email at newadapter@realtimeresults.net, or online at www.skylightframe.com and click on Product Recall Information at the bottom of the page for more information.

      Skylight of San Francisco, Calif., is recalling about 65,000 Series I power adapters for Skylight digital photo frames sold in the U.S., and Canada.The...
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      Forest River recalls Sunseekers, Freelanders and Leprechauns

      The seatbelt-unfastened warning light is slow to illuminate

      Forest River is recalling six model year 2020 Sunseeker SSC2250SLEC, Freelander FLC26RSC, and Leprechaun LPC240FSC vehicles.

      The seatbelt-unfastened warning light will not illuminate for approximately five seconds after the ignition is moved to the "on" or "start" position.

      Without the seatbelt warning reminder, the driver may forget to fasten the seatbelt, increasing the risk of injury in a crash.

      What to do

      Forest River will notify owners, and GM dealers will reprogram the instrument panel, free of charge.

      The recall began on October 29, 2019.

      Owners may contact GMC customer service at (800) 462-8782 or Forest River customer service at (800) 348-7440. Forest River's number for this recall is 51-1084.

      Forest River is recalling six model year 2020 Sunseeker SSC2250SLEC, Freelander FLC26RSC, and Leprechaun LPC240FSC vehicles.The seatbelt-unfastened war...
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      Skacel Collection recalls FlipStix knitting needles

      The shaft of the knitting needle can split or burst, posing a laceration hazard.

      Skacel Collection of Seattle, Wash., is recalling about 270 US 6 (4.0mm) addi FlipStix knitting needles.

      The shaft of the knitting needle can split or burst, posing a laceration hazard.

      The firm has received three reports of the needle shafts splitting. No injuries have been reported.

      This recall involves US 6 (4.0mm diameter) FlipStix in 6” and 8” long knitting needles.

      The knitting needles have aluminum shafts that are tapered at both ends. The long shaft holds the active (unsecured) stitches of the fabric, to prevent them from unravelling, whereas the tapered ends are used to form new stitches. The knitting needles were sold in blue, red and yellow combination packages, with five needles per pack.

      The needles, manufactured in Germany, were sold at independent yarn stores nationwide from November 2018, through August 2019, for about $20.

      What to do

      Consumers should immediately stop using the recalled knitting needles and contact the store where purchased for a full refund in the form of a store voucher.

      Consumers may contact Skacel Collection at (800) 255-1278 from 8 a.m. to 3:30 p.m. (PT) Monday through Friday, by email at recall@skacelknitting.com or online at www.skacelknitting.com/FlipStix_US6_Recall_Info for more information.

      Skacel Collection of Seattle, Wash., is recalling about 270 US 6 (4.0mm) addi FlipStix knitting needles.The shaft of the knitting needle can split or b...
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      Mann Packing recalls veggies

      The products may be contaminated with Listeria monocytogenes

      Mann Packing Co., is recalling a series of vegetable products sold to select retailers in the U.S. and Canada.

      The products may be contaminated with Listeria monocytogenes.

      There are no reported illnesses to date.

      Lists of the recalled products, with “Best If Enjoyed By” dates of October 11, 2019, to November 16, 2019, are available here and here.

      What to do

      Customers who purchased the recalled products should discard them.

      Consumers with questions may call customer service 24/7 at (844) 927-0707 or by email at consumers@mannpacking.com.

      Mann Packing Co., is recalling a series of vegetable products sold to select retailers in the U.S. and Canada.The products may be contaminated with Lis...
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      Ducati recalls Hypermotard 950 and 950 SP motorcycles

      The motorcycle may abruptly lose power and stall

      Ducati North America is recalling 793 model year 2019-2020 Hypermotard 950 and 950 SP motorcycles.

      The negative terminal on the battery may break, potentially causing a sudden loss of power and an engine stall, which can increase the risk of a crash.

      What to do

      Ducati will notify owners, and dealers will inspect the routing of the negative cable, rerouting it as necessary. In addition, the battery will be better secured with insulation pads. These repairs will be performed free of charge.

      The recall is expected to begin December 12, 2019.

      Owners may contact Ducati customer service at (888) 391-5446. Ducati's number for this recall is SRV-RCL-19-003.

      Ducati North America is recalling 793 model year 2019-2020 Hypermotard 950 and 950 SP motorcycles.The negative terminal on the battery may break, poten...
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      Porsche recalls vehicles with electrical issue

      The instrument cluster may not provide a visual warning of worn brake pads

      Porsche Cars North America is recalling 44,128 of the following vehicles, superseding an earlier recall:

      • Model year 2017 Panamera 4, Panamera Turbo & Panamera Turbo Executive
      • Model year 2017-2018 Panamera, Panamera 4S Executive & Panamera 4S
      • Model year 2018 Panamera Turbo S Hybrid, Panamera 4 Hybrid Sport Turismo, Panamera 4 Sport Turismo, Panamera Turbo S Hybrid Sport Turismo, Panamera 4 Hybrid & Panamera 4 Executive,
      • Model year 2019 Cayenne Hybrid
      • Model year 2019-2020 Cayenne, Cayenne S & Cayenne Turbo, and
      • Model year 2020 Cayenne Coupe, Cayenne Turbo Coupe, & Cayenne S Coupe

      The instrument cluster may not provide a visual warning when the brake pads are worn out.

      If the driver is not alerted when brake pads are worn out, the vehicle may not respond as expected when braking, increasing the risk of crash.

      What to do

      Porsche will notify owners, and dealers will reprogram the instrument cluster free of charge.

      The recall is expected to begin December 15, 2019.

      Owners may contact Porsche customer service at (800) 767-7243. Porsche's number for this recall is AKB8.

      Porsche Cars North America is recalling 44,128 of the following vehicles, superseding an earlier recall: Model year 2017 Panamera 4, Panamera Turbo &...
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      Wawona Frozen Food recalls frozen raspberries

      The products may be contaminated with Hepatitis A

      Wawona Frozen Foods is recalling packages of frozen raspberries and frozen berry mixes containing raspberries.

      The products may be contaminated with Hepatitis A.

      No illnesses have been reported to date.

      The following products, imported from Chile and sold at Adi and Raley stores, are being recalled:

      • Season's Choice Raspberries (frozen): 12 ounce bags, "best by" date of June, 10, 2021, August 1,2021 and August 23, 2021. "Product of Chile." UPC Code: 0 41498 12419 9
      • Season's Choice Berry Medley (frozen) containing raspberries: 16 ounce bags, "best by" date of July 17, 2021, July 20, 2021 and July 22, 2021. "Product of USA, Chile." UPC Code: 0 41498 31344 9
      • Raley's Fresh Frozen Red Raspberries: 12 ounce bags, "best by" date of June 5, 2021 (lot code:20156A04), August 1, 2021 (lot code: 20213A06) "Product of Chile." UPC Code: 46567 00754

      What to do

      Customers who purchased the recalled products should not consume them, but discard or return them to the place of purchase for a full refund.

      Consumers with questions may contact Wawona Frozen Foods at (866) 913-0667 or online at www.wawona.com.

      Wawona Frozen Foods is recalling packages of frozen raspberries and frozen berry mixes containing raspberries.The products may be contaminated with Hep...
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      Polaris recalls model year 2015-2019 Slingshot motorcycles

      The motorcycle could lose electrical power

      Polaris is recalling 31,987 model year 2015-2019 Slingshot motorcycles.

      Excessive electrical current may damage the battery fuse holder terminals.

      Damaged terminals may result in the loss of forward and rear lighting, instrument cluster gauges or power steering assist, any of which could increase the risk of a crash.

      What to do

      Polaris will notify owners, and dealers will inspect the battery fuse block terminals and relocate the 50 amp chassis fuse free of charge.

      The recall was expected to begin in October 2019.

      Owners may contact Polaris customer service at (855) 863-2284. Polaris's number for this recall is T-19-01.

      Polaris is recalling 31,987 model year 2015-2019 Slingshot motorcycles.Excessive electrical current may damage the battery fuse holder terminals.Da...
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      H&T Seafood recalls Swai filets

      The product was imported without undergoing USDA inspection

      H&T Seafood of Bell, Calif., is recalling an undetermined amount of Siluriformes products (Swai filets).

      The products, imported from Vietnam, were packed and distributed without undergoing USDA inspection, and used the mark of inspection without authorization.

      There are no confirmed reports of adverse reactions.

      The following frozen item, produced over an undetermined amount of time, is being recalled:

      • 1-lb. plastic bags containing frozen fillets of “FISHERMAN’S WHARF SWAI FILLETS PRODUCT OF VIETNAM” with any USDA mark of inspection.

      The recalled product was shipped to warehouse/distribution centers and retail locations in Florida, Georgia, Louisiana and South Carolina.

      What to do

      Customers who purchased the recalled product should not consume it, but discard or return it to the place of purchase.

      Consumers with questions may contact Dat Huynh at (626) 679-1776.

      H&T; Seafood of Bell, Calif., is recalling an undetermined amount of Siluriformes products (Swai filets).The products, imported from Vietnam, were pack...
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      Lannett recalls Ranitidine Syrup

      The medication is contaminated with a probable cancer-causer

      Lannett Company is recalling all lots of Ranitidine Syrup.

      The product is contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

      The recalled product is used as a short-term treatment for active duodenal ulcers, maintenance therapy for duodenal ulcer patients, treatment of pathological hypersecretory conditions, short-term treatment of active, benign gastric ulcers, maintenance therapy for gastric ulcers, treatment of GERD and treatment of endoscopically diagnosed erosive esophagitis.

      The following lots of the product, packaged in bottles of 16 fluid ounces (one pint) (NDC 54838-550-80), are being recalled:

      NDC CodeBatch   Expiration Date 
      54838-550-801503A10/2019
      54838-550-801504A10/2019
      54838-550-801505A10/2019
      54838-550-801523A10/2019
      54838-550-801524A10/2019
      54838-550-801525A11/2019
      54838-550-801561A12/2019
      54838-550-801562A12/2019
      54838-550-801563A12/2019
      54838-550-801589A12/2019
      54838-550-801590A12/2019
      54838-550-801591A12/2019
      54838-550-801614A01/2020
      54838-550-801615A01/2020
      54838-550-801617A01/2020
      54838-550-801644A02/2020
      54838-550-801775A06/2020
      54838-550-801794A06/2020
      54838-550-801795A06/2020
      54838-550-801796A06/2020
      54838-550-801817A06/2020
      54838-550-801818A07/2020
      54838-550-801819A07/2020
      54838-550-801840A08/2020
      54838-550-801840B08/2020
      54838-550-801841A08/2020
      54838-550-801842A08/2020
      54838-550-801863A08/2020
      54838-550-801864A09/2020
      54838-550-801865A09/2020
      54838-550-801899A10/2020
      54838-550-801900A10/2020
      54838-550-801901A10/2020
      54838-550-801910A10/2020
      54838-550-801911A10/2020
      54838-550-801912A10/2020
      54838-550-801918A10/2020
      54838-550-801919A10/2020
      54838-550-801920A10/2020
      54838-550-801925A10/2020
      54838-550-801926A10/2020
      54838-550-801927A10/2020
      54838-550-801977A12/2020
      54838-550-801978A12/2020
      54838-550-801979A12/2020
      54838-550-801646A02/2020
      54838-550-801647A02/2020
      54838-550-801668A03/2020
      54838-550-801669A03/2020
      54838-550-801670A03/2020
      54838-550-801708A03/2020
      54838-550-801709A04/2020
      54838-550-801710A04/2020
      54838-550-801729A04/2020
      54838-550-801730A04/2020
      54838-550-801731A04/2020
      54838-550-801757A05/2020
      54838-550-801758A05/2020
      54838-550-801759A05/2020
      54838-550-801773A06/2020
      54838-550-801774A06/2020
      54838-550-801989A12/2020
      54838-550-801990A12/2020
      54838-550-801991A12/2020
      54838-550-801998A01/2021
      54838-550-801999A01/2021
      54838-550-802000A01/2021
      54838-550-802019A01/2021
      54838-550-802020A01/2021
      54838-550-802065A03/2021
      54838-550-802066A03/2021
      54838-550-802067A03/2021
      54838-550-802071A03/2021
      54838-550-802072A03/2021
      54838-550-802073A03/2021
      54838-550-802076A03/2021
      54838-550-802077A03/2021
      54838-550-802078A03/2021
      54838-550-802126A05/2021
      54838-550-802127A05/2021
      54838-550-802128A05/2021
      54838-550-802164A06/2021
      54838-550-802165A06/2021
      54838-550-802166A06/2021
      54838-550-802179A06/2021
      54838-550-802180A07/2021
      54838-550-802181A07/2021
      54838-550-802214A08/2021
      54838-550-802215A08/2021
      54838-550-802216A08/2021

      The recalled product was distributed nationwide to wholesalers/distributors.

      What to do

      Patients should contact their physician or healthcare provider if they have any problems that may be related to taking or using the recalled product.

      Lannett Company is recalling all lots of Ranitidine Syrup.The product is contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen,...
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      John Deere recalls compact utility tractors

      Improperly torqued front cab support bolts can fail during a rollover

      Deere & Company of Moline, Ill., is recalling about 8,500 John Deere 4044R, 4052R and 4066R compact utility tractors sold in the U.S., and Canada.

      Front cab support bolts that were torqued improperly during manufacturing can fail during a rollover, posing a crushing injury hazard to the operator.

      No incidents or injuries are reported.

      This recall involves green and yellow compact utility tractors with “John Deere” and the model numbers 4044R, 4052R or 4066R printed on the hood.

      Each of the recalled compact utility tractors has a 17-digit serial number located on the right side of the frame above the front axle.

      Each serial number included in the recall begins with “1LV” and ends with a six-digit number that falls within the ranges below:

      Model             Serial Number Range

      4044R             400284 - 401619

      4052R             400381 – 403424

      4066R             401588 - 407220

      The tractors, manufactured in the U.S., were sold at John Deere dealers nationwide from October 2016, through September 2019, for between $40,000 and $50,000.

      What to do

      Consumers should immediately stop using the recalled compact utility tractors and contact an authorized John Deere dealer for a free repair. John Deere is contacting all known purchasers directly.

      Consumers may contact Deere & Company at (800) 537-8233 from 8 a.m. to 6 p.m. (ET) Monday through Friday, and 9 a.m. to 3 p.m. (ET) on Saturday, or online at www.deere.com and click on “Recalls” on the drop-down menu under “Parts & Services” at the top of the page for more information.

      Deere & Company of Moline, Ill., is recalling about 8,500 John Deere 4044R, 4052R and 4066R compact utility tractors sold in the U.S., and Canada.Front...
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      Golden Dragon Fortune Cookies recalls Chinese Almond Cookies

      The product may contain milk, an allergen not declared on the label

      Golden Dragon Fortune Cookies of Chicago, Ill., is recalling Golden Dragon Chinese Almond Cookies.

      The product may contain milk, an allergen not declared on the label.

      No illnesses have been reported to date.

      The recalled product is packaged in 5-lbs. boxes that contain five, 100-count plastic bags of the Almond Cookies. It may have been purchased by consumers in either the 5-lbs. box or the 100-count plastic bags. Both have UPC code 0 80005 23031 2 and Best if Used Before 3/20.

      The cookies were sold by retail stores and wholesalers in Chicago, Ill.

      What to do

      Customers who purchased the recalled product should return it to the place of purchase for a full refund.

      Consumers with questions may contact the company at (312) 842-8199 Monday through Friday, 8AM to 5PM.

      Golden Dragon Fortune Cookies of Chicago, Ill., is recalling Golden Dragon Chinese Almond Cookies.The product may contain milk, an allergen not declare...
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      North Bay Produce recalls fresh apples

      The products may be contaminated with Listeria monocytogenes

      North Bay Produce of Traverse City, Mich., is recalling 2,297 cases and two bulk bins of fresh apples.

      The products may be contaminated with Listeria monocytogenes.

      No illnesses have been linked by health officials to this recall.

      Recalled varieties include McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples sold in plastic bags under the Great Lakes, North Bay Produce Pure Michigan brands, as well as unbranded in clear plastic tote bags, white paper tote bags, and individually from retailers display trays.

      The recalled products were shipped between October 16 – 21, 2019, from one North Bay facility to wholesalers, retailers and brokers in Florida, Illinois, Kentucky, Louisiana, Michigan, North Carolina, Texas and Wisconsin.

      The following products are being recalled:

      Distributed ByVariety, Brand & PackagingArrival Date(s)UPC CodePLU
      Number
      Item
      Number
      Shipped-To- Location
      North Bay
      Produce, Inc.
      McIntosh Great
      Lakes 3lb. Plastic
      Bag, Product of MIUSA
      Delivered between 10/19/19 and 10/21/198 13635
      01012 8
      Michigan Louisiana
      North Bay
      Produce, Inc.
      Jonathan
      Great Lakes 3lb. Plastic Bag, Product of MI-USA
      Delivered 10/21/198 13635
      01017 3
      Louisiana
      North Bay
      Produce, Inc.
      Honeycrisp Great
      Lakes 3lb. Plastic
      Bag, Product of MI- USA/span>
      Delivered 10/21/198 13635
      01018 0
      Louisiana
      North Bay
      Produce, Inc.
      Jonamac Great
      Lakes 3lb. Plastic
      Bag, Product of MIUSA
      Delivered 10/16/198 13635
      01019 7
      Wisconsin
      North Bay
      Produce, Inc.
      McIntosh North Bay Pure Michigan 3lb. Plastic Bag, Product of MI-USADelivered 10/21/198 13635
      01012 8
      Michigan
      North Bay
      Produce, Inc.
      Honeycrisp North
      Bay Pure Michigan
      2lb. Plastic Bag,
      Product of MI-USA
      Delivered 10/19/198 13635
      01130 9
      Michigan
      North Bay
      Produce, Inc.
      Honeycrisp Quarter
      Peck Paper Tote
      Bag, Product of MI - USA
      Delivered 10/19/19700116Michigan
      North Bay
      Produce, Inc.
      Fuji
      Half Peck Plastic Tote Bags, Product of MI-USA
      Delivered 10/18/194195All Fresh Thyme
      Farmers Market
      Stores
      North Bay
      Produce, Inc.
      Jonathan Bulk 600lb
      Corugated Bins,
      Product of MI-USA
      Delivered 10/16/19Michigan
      North Bay
      Produce, Inc.
      Mcintosh
      Distributed in trays;
      Product of MI-USA
      Delivered
      10/19/19 &
      10/21/19
      4019Not sold at retail
      North Bay
      Produce, Inc.
      Red Delicious Distributed in trays; sold individually for retail sale, Product of MI-USADelivered 10/21/194168
      4167
      North Carolina
      Department of
      Agriculture (Food
      Distribution
      Division- Butner)
      Creedmoor, North Carolina
      Feeding South
      Florida
      Pembroke Park,
      Florida

      Apples purchased at retail prior to October 16th are not affected.

      What to do

      Customers who purchased the recalled products should not consume them, but discard or return them to the place of purchase.

      Consumers with questions may contact the company at (231-929-4001, Monday-- Friday, 8am -- 5pm (ET) or online at www.northbayproduce.com.

      North Bay Produce of Traverse City, Mich., is recalling 2,297 cases and two bulk bins of fresh apples.The products may be contaminated with Listeria mo...
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      Forest River recalls model year 2020 Shasta Oasis trailers

      The axle may contact the chassis while the trailer is moving

      Forest River is recalling 44 model year 2020 Shasta Oasis SST30QB and SST31OK trailers.

      The trailers may have been built with an incorrect length axle hanger, allowing the axle to contact the chassis while the trailer is moving.

      The axle hanger contacting the chassis can cause loss of vehicle control, increasing the risk of a crash.

      What to do

      Forest River will notify owners, and dealers will replace the equalizers free of charge.

      The recall is expected to begin November 25, 2019.

      Owners may contact Forest River customer service at (574) 528-8717. Forest River's number for this recall is 53-1100.

      Forest River is recalling 44 model year 2020 Shasta Oasis SST30QB and SST31OK trailers.The trailers may have been built with an incorrect length axle h...
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      Novitium Pharma recalls Ranitidine Hydrochloride capsules

      The medication, used for treatment of gastric disorders, is contaminated with a probable cancer-causer

      Novitium Pharma is recalling all quantities and lots of Ranitidine Hydrochloride capsules in the U.S.

      The product is contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

      The recalled product is used for treatment of duodenal ulcer, benign gastric ulcer, reflux esophagitis, post-operative peptic ulcer, Zollinger-Ellison Syndrome, and other conditions where reduction of gastric secretion and acid output is desirable.

      The following products are being recalled: 

      Description

      Strength

      Type

      Pack Size

      NDC

      Ranitidine Capsules 150mg150 mgRx60 ct bottle70954-001-20
      Ranitidine Capsules 150mg150 mgRx500 ct bottle70954-001-40
      Ranitidine Capsules 300mg300 mgRx30 ct bottle70954-002-10
      Ranitidine Capsules 300mg300 mgRx100 ct bottle70954-002-40

      What to do

      Patients should continue taking their medication and speak to their physician or pharmacist about alternate healthcare treatment options. Customers desiring to return product should contact the pharmacy from which it was purchased.

      Consumers with questions may contact the company at (609) 469-5920 or by email at info@novitiumpharma.com.

      Novitium Pharma is recalling all quantities and lots of Ranitidine Hydrochloride capsules in the U.S.The product is contaminated with N-Nitrosodimethyl...
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      Arcimoto FUV motorcycles recalled

      The tie rod assembly may separate

      Arcimoto is recalling ten Arcimoto FUV motorcycles.

      There may be insufficient thread engagement between the inner and outer tie rods, possibly resulting in the separation of the tie rod assembly.

      A tie rod separation can cause a loss of steering and increase the risk of a crash.

      What to do

      Arcimoto is still finalizing a remedy to better secure the tie rods free of charge.

      Owners may contact Arcimoto customer service at (541) 683-6293.

      Arcimoto is recalling ten Arcimoto FUV motorcycles.There may be insufficient thread engagement between the inner and outer tie rods, possibly resulting...
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