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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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      Mazda recalls CX-9s with Sumitomo Falken tires

      The tire tread may separate and detach

      Mazda North American Operations is recalling 146 model year 2019 CX-9s equipped with Sumitomo Falken ZIEX CT50 A/S tires, size P255/50R20 104V -- date code 1619.

      An incorrect rubber compound may have been used in the tire's manufacturing, allowing the tread to separate and detach.

      A detached tire tread can decrease vehicle stability and increase the risk of a crash.

      What to do

      Mazda will notify owners, and dealers will inspect all four tire serial numbers, replacing the tires as necessary 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 4019J.

      Mazda North American Operations is recalling 146 model year 2019 CX-9s equipped with Sumitomo Falken ZIEX CT50 A/S tires, size P255/50R20 104V -- date code...
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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)...
      Read lessRead more