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    C3 Manufacturing recalls Perfect Descent Climbing Systems climbing belay devices

    The device can loosen and cause slack on the rope, allowing a climber to fall

    C3 Manufacturing of Littleton, Colo., is recalling about 1.200 Perfect Descent Auto Belays climbing devices.

    The belay climbing device can loosen and cause slack on the rope, allowing the climber to fall. Climbing while tethered to a malfunctioning belay can cause serious injury or death.

    No incidents or injuries are reported.

    This recall involves Perfect Descent Auto Belay model 220 Indoor, Outdoor, Speed Drive and Direct Drive auto belay climbing devices.

    Belay devices are used with climbing ropes to protect the climber while climbing, to arrest a fall or while being lowered on the rope.

    The devices were sold in yellow and black and have “Perfect Descent” printed on the top of the devices.

    The recalled belay devices have the following serial number ranges printed on the bottom of the device:

    Serial number                  Manufacture Date:

    I-0970 through I-3109      February 2017 through November 2018

    S-0604 through S-1609    March 2017 through December 2018 

    S-1695 through S-1762    February 2019 through March 2019 

    D-1015 through D-1385   June 2018 through December 2018 

    D-1572 through D-1705   February 2019 through March 2019 

    D-1710 through D-1722   March 2019

    D-1726 through D-1751   March 2019 through April 2019 

    D-1761 through D-1777   April 2019

    The climbing devices, manufactured in the U.S., were sold at Aerial Adventure Technologies nationwide and online at www.perfectdescent.com from February 2017, through April 2019, for $1,800 and $2,100.

    What to do

    Consumers should immediately stop using the recalled belay devices and contact C3 Manufacturing to receive a free repair. The firm contacted all known purchasers directly on October 21, 2019.

    Consumers may contact C3 Manufacturing toll-free at (866) 250-5903 from 9 a.m. to 6 p.m. (MT) Monday through Friday, by email at support@PerfectDescent.com or online at www.perfectdescent.com/product-notices/ for more information.

    C3 Manufacturing of Littleton, Colo., is recalling about 1.200 Perfect Descent Auto Belays climbing devices.The belay climbing device can loosen and ca...
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    Belle Chemical recalls drain cleaner

    The product label lacks the mandatory hazard statement on the front of the package

    Belle Chemical of Billings, Mont., is recalling about 6,400 containers of 100% Sodium Hydroxide Drain Cleaner.

    The label of the product, which contains sodium hydroxide, violates the Federal Hazardous Substance Act (FHSA) by omitting the word “poison” for poisonous chemicals and the mandatory hazard statement on the front on the packaging.

    No incidents or injuries are reported.

    This recall involves sodium hydroxide drain cleaner sold in a 2-lb white plastic bottle with a red and black label and includes a child-resistant closure.

    Belle Chemical, Sodium Hydroxide and 100% Sodium Hydroxide Drain Cleaner are printed on the label.

    The drain cleaner, manufactured in the U.S., was sold online at  Amazon.com, Walmart.com, Ebay.com, Bonanza.com, Jet.com, Etsy.com and Bellechemical.com from February 2017, through January 2020, for between $5 and $8.

    What to do

    Consumers should immediately store the recalled product in a safe location out of reach of children and contact Belle Chemical for a free replacement label to put on the product.

    Consumers may contact Belle Chemical toll-free at (877) 522-2233 from 8 a.m. to 4 p.m. (MT) Monday through Friday, by email at info@bellechemical.com or online at www.bellechemical.com and click on RECALL INFORMATION for more information.

    Belle Chemical of Billings, Mont., is recalling about 6,400 containers of 100% Sodium Hydroxide Drain Cleaner.The label of the product, which contains...
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    Novartis recalls Sandimmune and Neoral prescription drug blister packages

    The packaging is not child-resistant as required by law

    Novartis Pharmaceuticals of East Hanover, N.J., is recalling about 73,000 packages of Sandimmune soft gelatin capsules and Neoral soft gelatin capsules prescription drug blister packages.

    The prescription drug packaging is not child resistant as required by the Poison Prevention Packaging Act (PPPA), posing a risk of poisoning if the contents are swallowed by young children.

    No incidents or injuries are reported.

    This recall involves blister packages of prescription medications Sandimmune (cyclosporine capsules, USP) 100 mg soft gelatin capsules and Neoral (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules from Novartis.

    Packages of Sandimmune 100 mg contain three blister cards with ten soft gelatin capsules per card and packages of Neoral 100 mg contain five blister cards with six soft gelatin capsules per card.

    The recalled blister packages have “Novartis,” the name of the medication, dosage, NDC, lot number and expiration date on the outer package and on the blister cards.

    Only 100 mg doses of these medications with the following NDC and lot numbers and expiration dates are included in this recall:

    Recalled Prescription Drugs

    NDC Numbers

    Lot Numbers

    Expiration Date

    Sandimmune® (cyclosporine capsules, USP) 100 mg soft gelatin capsules

    0078-0241-15

    0078-0241-61

    APCA136

    APCA339

    APCA793

    APCC238

    09/2020

    02/2021 01/2022

    07/2022

    Neoral® (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules

    0078-0248-15

    0078-0248-61

    APCA437

    APCA979

    07/2020

    03/2021

    The medications, manufactured in the U.S., were sold at clinics and pharmacies nationwide as a prescribed medicine from March 2018, through March 2020, at prices varying based on quantities prescribed, health insurance terms, and other factors.

    What to do

    Consumers should immediately move the product out of the sight and reach of children and contact the firm to request a free child-resistant pouch in which to store the blister package medications. Consumers can continue to use the medication as directed. The child-resistant pouches should be used to store these medications until new child-resistant blister packaging is available.

    Consumers may contact Novartis toll-free at (866) 629-6182 from 8 a.m. to 8 p.m. (ET) daily, by email at Novartis5060@stericycle.com or online at https://www.pharma.us.novartis.com/news/statements/corrective-action-certain-100-mg-sandimmune-and-neoral-blister-packages-us for more information.

    Novartis Pharmaceuticals of East Hanover, N.J., is recalling about 73,000 packages of Sandimmune soft gelatin capsules and Neoral soft gelatin capsules pre...
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      SeeNext Venture recalls NumbSkin pain relief cream

      The packaging is not child resistant as required by federal law

      SeeNext Venture of Blaine, Wash., is recalling about 8,000 packages of NumbSkin pain relief cream with lidocaine.

      The packaging is not child resistant as required by the Poison Prevention Packaging Act.

      The pain relieving cream contains lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.

      No incidents or injuries are reported.

      This recall involves NumbSkin pain relief cream with 5% lidocaine, a topical anesthetic cream sold in 30 grams in a white with blue tube.

      NumbSkin is printed on the tube. Lot 9238 and a date code of 10/2019 through 09/2020 in a MM/YYYY format is embossed on the tub’s thin end. Batch number 9238 is printed on the product packaging.

      The pain relief cream, manufactured in Canada, was sold online at Amazon.com from October 2019 through February 2020 for about $25.

      What to do

      Consumers should immediately store the pain relief cream in a safe location out of reach of children and contact SeeNext Venture for instructions on how to dispose or return it and to receive a free replacement similar product with a child-resistant cap. Amazon is contacting all known purchasers directly.

      Consumers may contact SeeNext Venture toll-free at (844) 700-6862 from 9 a.m. to 6 p.m. (PT) Monday through Saturday, by email at distributions@numbskin.com or online at www.numbskin.com and click on “Recall” at the top of the page for more information.

      SeeNext Venture of Blaine, Wash., is recalling about 8,000 packages of NumbSkin pain relief cream with lidocaine. The packaging is not child resistant a...
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      Boyer recalls six brands of sodium and potassium hydroxide

      The packaging of the products is not child resistant

      The Boyer Corporation of LaGrange, Ill., is recalling about 329,000 packages of Soap Supply Co. Lye, Soap Makers Lye, California Soap Supply, Combo Pure Solutions, Red Crown High Test Lye, and Boyer Potassium Hydroxide Flakes.

      The products contain sodium and/or potassium hydroxide which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA).

      The packaging of the products is not child resistant, posing a risk of chemical burns and irritation to the skin and eyes.

      CPSC has received two reports of chemical burn injuries the California Soap Supply product. One involved a child who received chemical burns to his mouth after gaining access to the product.

      This recall involves six brands of sodium and potassium hydroxide products sold in two pound clear plastic bottles with a continuous thread closure cap.

      The products are commonly advertised as being used for home soapmaking projects and clearing drains.

      The lot numbers included in the recall are from 4001 to 9288 and are located on the bottom of the jar and on the side of the box. 

      The brands of products and description of the packaging included in the recall are:

      Brand

      Description 

      Distributed By 

      Soap Supply Co. Lye 

      yellow label

      BigTProducts

      Soap Makers Lye

      green label

      BigTProducts

      California Soap Supply 

      dark blue label

      NG Inc.

      Combo Pure Solutions

      light blue label

      NG Inc.

      Red Crown High Test Lye

      red label

      Boyer Corporation

      Boyer Potassium Hydroxide Flakes

      white label

      Boyer Corporation

      The recalled products, manufactured in the U.S., were sold online at Amazon.com and other websites from January 2015, through October 2019, for about $5.

      What to do

      Consumers should immediately store the recalled products in a safe location out of reach of children and contact Boyer for a free replacement child-resistant cap.

      Consumers may contact Boyer Corporation at (800) 323-4030 from 9 a.m. to 4 p.m. (ET) Monday through Friday, by email at boyer9600@gmail.com or online at www.boyercorporation.com.

      The Boyer Corporation of LaGrange, Ill., is recalling about 329,000 packages of Soap Supply Co. Lye, Soap Makers Lye, California Soap Supply, Combo Pure So...
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      Natural Remedy recalls Active Male

      The dietary supplement for male enhancement contains tadalafil not declared on the label

      Natural Remedy Store is recalling all lots of Active Male.

      FDA analysis has found the product is tainted with tadalafiln is an FDA-approved drug indicated for the treatment of male erectile dysfunction, not declared on the label.

      That makes it an unapproved drug for which safety and efficacy has not been established.

      There are no reports of adverse events to date.

      The recalled product, in 500-mg capsules is packaged in small foldable cardboard with the image of a Trojan helmet and the name Active Male with BN: Nd6332.

      It was sold at the Natural Remedy Store in San Antonio Texas, and through the company's website.

      What to do

      Customers who purchased the recalled product should stop using it t and return it to place of purchase and/or call the firm to arrange for return.

      Consumers with questions may contact Natural Remedy Store at (210) 798-5433 Monday thru Saturday, 10:00AM to 6:00PM (CT) or by e-mail at natremedies@att.net.

      Natural Remedy Store is recalling all lots of Active Male. FDA analysis has found the product is tainted with tadalafiln is an FDA-approved drug indicat...
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      Raw Seafoods recalls Wegmans brand Oven Safe Salmon Teriyaki and Ginger Salmon

      The products contain wheat, an allergen not declared on the label

      Raw Seafoods Inc. is recalling  Wegmans brand Ginger Salmon Oven Safe Meal and Salmon Teriyaki Oven Safe Meal.

      The products contain wheat, an allergen not declared on the label.

      No illnesses or allergic reactions are reported to date.

      The following products, distributed to Wegmans stores in New York, Massachusetts, New Jersey, Pennsylvania, Maryland, Virginia and North Carolina, are being recalled:

      Product Name and PLU CodeCode on PackagingBest By Date
      Wegmans Ginger Salmon, Oven Safe - 6474760801/23/2021
      765902/13/2021
      Wegmans Salmon Teriyaki, Oven Safe - 6408768802/24/2021
      769202/25/2021

      The product code and best by date are listed in the bottom right corner on the front facing label.

      What to do

      Customers who purchased the recalled products and have an allergy to wheat should not consume them, but return them to the place of purchase.

      Consumers with questions may contact the company at (508) 673-0111, Monday – Friday from 8am to 5pm (EST).

      Raw Seafoods Inc. is recalling  Wegmans brand Ginger Salmon Oven Safe Meal and Salmon Teriyaki Oven Safe Meal. The products contain wheat, an allergen n...
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      Heartland recalls model year 2020 Shadow Cruiser Ultra Lite trailers

      The certification label contains incorrect GVWR information

      Heartland Recreational Vehicles is recalling five model year 2020 Shadow Cruiser Ultra Lite trailers.

      The certification label indicates an incorrect GVWR and axle rating.

      An incorrect GVWR could result in the vehicle being overloaded and the axles failing, increasing the risk of a crash.

      What to do

      Heartland will notify owners and send them corrected replacement labels, free of charge.

      The recall is expected to begin May 11, 2020.

      Owners may contact Heartland customer service at (877) 262-8032.

      Heartland Recreational Vehicles is recalling five model year 2020 Shadow Cruiser Ultra Lite trailers.The certification label indicates an incorrect GVW...
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      AFC recalls Cooked Butterfly Tail-On Whiteleg Shrimp

      The product may be contaminated with Vibrio parahaemolyticus

      AFC Distribution Corp. of Rancho Dominguez, Calif., is recalling Cooked Butterfly Tail-On Whiteleg Shrimp (Sushi Ebi).

      The product may be contaminated with Vibrio parahaemolyticus, an organism that can cause illnesses such as nausea, vomiting, diarrhea, fever and chills.

      There are no confirmed illnesses to date.

      The recalled product, Lot #2019.10.02 with sell-by dates ranging from 02/19/2020 to 03/13/2020.

      It was shipped to designated retail AFC sushi counters, where it is further processed into prepared sushi items, within grocery stores, cafeterias, and corporate dining centers in Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Florida, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Mexico, New York, Ohio, Oregon, Pennsylvania, Soth Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia and Wyoming.

      What to do

      Customers who purchsed the recalled product to discard or return it to the place of purchase for a full refund.

      Consumers with questions may contact AFC at (866)467-8744 Monday – Friday, 8:00 AM to 5:00 PM (PT) or by email at recall@afcsushi.com.

      AFC Distribution Corp. of Rancho Dominguez, Calif., is recalling Cooked Butterfly Tail-On Whiteleg Shrimp (Sushi Ebi). The product may be contaminated w...
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      Winco Foods recalls frozen blackberries and frozen berry medley

      The products may be contaminated with Norovirus

      WinCo Foods of Boise, Idaho, is recalling frozen blackberries and frozen berry medley manufactured by Rader Farms of Lynden, Wash.

      The products may be contaminated with a highly contagious Norovirus.

      No customer illnesses have been reported to date.

      The following products with a “Best By Code” is located on the front of the package, are being recalled:

      • WINCO FOODS FROZEN BLACKBERRIES, 16 OZ. BAG – UPC: 70552-30502, Best By Code Dec/09/2021.
      • WINCO FOODS FROZEN BERRY MEDLEY, 16 OZ. BAG – UPC: 70552-30522, Best By Code Dec/09/2021.
      • WINCO FOODS FROZEN BERRY MEDLEY, 32 OZ. BAG – UPC: 70552-30512, Best By Code Dec/09/2021.

      Te recalled products were distributed to WinCo Foods stores in Arizona, California, Idaho, Montana, Nevada, Oklahoma, Oregon, Washington, Texas and Utah.

      What to do

      Customers who purchased the recalled products should discard or return them to the store for a full refund.

      Consumers with questions may contact the company at (800) 824-1706 Monday – Friday, 7:30 – 4:30 (MST).

      WinCo Foods of Boise, Idaho, is recalling frozen blackberries and frozen berry medley manufactured by Rader Farms of Lynden, Wash. The products may be c...
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      Joyson Safety Systems recalls rear seat belt retractors

      The seat belt may not restrain occupants

      Joyson Safety Systems is recalling 108,047 rear seat belt retractors equipped with a dual mode belt locking mechanism.

      Due to a manufacturing issue, the seat belt webbing locking mechanism may not properly restrain the occupant as intended.

      If the occupant is not properly restrained in a crash, there is an increased risk of injury.

      What to do

      Joyson will notify the vehicle manufacturers that purchased the seat belt retractors.

      Dealers for those companies will notify owners, and replace the rear retractor assemblies -- as necessary -- free of charge.

      Owners may contact Joyson customer service at (586) 726-3800. Joyson's number for this recall is QN3998.

      Joyson Safety Systems is recalling 108,047 rear seat belt retractors equipped with a dual mode belt locking mechanism. Due to a manufacturing issue, the...
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      Homestar recalls Finch dressers

      The dressers can tip over if they are not anchored to the wall

      Homestar North America of Dallas, Texas, is recalling about 33,000 Finch three-drawer dressers.

      The dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in death or injuries to children.

      No incidents or injuries are reported.

      This recall involves Homestar Finch three-drawer dressers in maple/bank adler (EB10873BA), black (EB108738Q), torino walnut (EB108738TW) and white (EB108738W), sold alone or as part of a matching bedroom collection.

      Homestar North America and the model number are printed on a label on the back of the recalled dressers. The contemporary style dressers have three drawers with three brushed nickel finish metal handles.

      The dressers measure 28 inches high, 27.5 inches wide, 16 inches deep and weigh about 47 pounds.

      The dressers, manufactured in the U.S., were sold online on Amazon.com, Hayneedle.com, Overstock.com, Walmart.com and other online retailers from January 2016, through May 2019, for about $90.

      What to do

      Consumers should immediately stop using any recalled dressers that are not properly anchored to the wall and place them in an area that children cannot access.

      Contact Homestar to receive a free tip-over restraint kit and a one-time free in-home installation of the kit. Homestar is contacting all known purchasers directly.

      Consumers may contact Homestar toll-free at (877) 353-5999 from 9 a.m. to 5 p.m. (ET) Monday through Friday, by email at CPSCanti-tip@homestarltd.com or online at www.homestar-finch-recall.com or www.homestarltd.com and click on “Recall Info Finch Dresser” at the bottom of the page.

      Homestar North America of Dallas, Texas, is recalling about 33,000 Finch three-drawer dressers. The dressers are unstable if they are not anchored to th...
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      Henry & Tenry Food Products recalls spring rolls

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

      Henry & Tenry Food Products Company is recalling its own brand of spring rolls that may contain milk, an allergen not declared on the label.

      There are no reported adverse reactions.

      The following items, sold in Canada's Albert province, are being recalled:

      BrandProductSizeUPCCodes
      Henry & Tenry
      Food Products
      Spring Roll50 piecesNoneAll units sold up to and including February 29, 2020 where milk is not declared on the label
      Henry & Tenry Food ProductsSpring Roll (L)25 piecesNoneAll units sold up to and including February 29, 2020 where milk is not declared on the label
      Henry & Tenry Food ProductsSpring Roll Veg (L)25 piecesNoneAll units sold up to and including February 29, 2020 where milk is not declared on the label
      NoneUnlabeled (spring rolls)50 rollsNoneAll units sold up to and including February 29, 2020 where milk is not declared on the label
      NoneUnlabeled (spring rolls (large))25 rollsNoneAll units sold up to and including February 29, 2020 where milk is not declared on the label
      NoneUnlabeled (vegetarian spring rolls (large))25 rollsNoneAll units sold up to and including February 29, 2020 where milk is not declared on the label

      What to do

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

      Consumers with questions may contact the company at (780) 421-0988.

      Henry & Tenry Food Products Company is recalling its own brand of spring rolls that may contain milk, an allergen not declared on the label. There are n...
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      Kichler Lighting recalls ceiling fans

      The arms that hold the ceiling fan blades can detach during use

      Kichler Lighting of Cleveland, Ohio, is recalling about 42,000 Kichler 52-inch LED indoor ceiling fans old in the U.S. and Canada.

      The irons (arms) that hold the ceiling fan blades can detach during use, causing the blades to fall, posing an injury hazard.

      The firm has received about 62 reports of the fan blade iron breaking or detaching, with one report of property damage. No injuries have been reported.

      This recall involves Kichler’s indoor ceiling fans with five blades, bronze accents, etched umber glass and an integrated LED module. The fans are 52 inches wide and have a Mediterranean Walnut finish. Model number 35153 is printed on the top of the fan’s motor housing.

      The fans, manufactured in China, were sold at Lowe’s and other lighting specialty stores nationwide and online at www.lowes.com from January 2016, through March 2020, for about $250.

      What to do

      Consumers should immediately stop using the recalled ceiling fans and contact Kichler for instructions on receiving a free replacement.

      Consumers may contact Kichler Lighting toll-free at (866) 558-5706 from 8 a.m. to 4:30 p.m. (ET) Monday through Friday or online at www.kichler.com and click on “Safety Information” at the bottom of the page for more information.

      Kichler Lighting of Cleveland, Ohio, is recalling about 42,000 Kichler 52-inch LED indoor ceiling fans old in the U.S. and Canada. The irons (arms) that...
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      Keystone recalls model year 2020 Bullet 34RI trailers

      The egress window in the main living area may be missing

      Keystone RV Company is recalling 27 model year 2020 Bullet 34RI trailers with overhead cabinets across the rear wall.

      The trailers may be missing an egress window in the main living area, preventing passenger exit in the event of an emergency.

      The missing egress window can lengthen the time passengers need to exit the vehicle, increasing the risk of injury.

      What to do

      Keystone will notify owners, and dealers will replace the existing crank open vent window with an egress window free of charge.

      The recall is expected to begin April 21, 2020.

      Owners may contact Keystone customer service at (866) 425-4369.

      Keystone RV Company is recalling 27 model year 2020 Bullet 34RI trailers with overhead cabinets across the rear wall. The trailers may be missing an egr...
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      Pero Family Farms recalls zucchini trays

      The product contains egg and milk, allergens not declared on the label

      Pero Family Farms Food Company is recalling its Zucchini Spiral Pesto Side Dish Kit.

      The product contains egg and milk, allergens not declared on the label.

      No illnesses have been reported to date.

      Th recalled product, packaged in an 11-oz flexible clear plastic container, with run number code 1196272F and Use By date of 03/20/2020, was sold under the Pero Family Farms Label in Florida, Alabama, Tennessee, South Carolina, North Carolina, Virginia and Georgia.

      The product run number code and use by date can be found on the front bottom right hand corner of the package.

      What to do

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

      Consumers with questions may contact Pero Family Farms Food at (561) 498-5771 from 8 am – 5pm Monday through Friday.

      Pero Family Farms Food Company is recalling its Zucchini Spiral Pesto Side Dish Kit. The product contains egg and milk, allergens not declared on the la...
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      Arcimoto recalls FUV motorcycles

      The motorcycles could lose drive power

      Arcimoto is recalling 66 model year 2019-2020 FUV motorcycles.

      The traction-power harnesses large-gauge cable-lugs may be uncrimped or improperly crimped.

      Uncrimped or improperly crimped cable lugs can cause loss of drive power, increasing the risk of a crash. In addition, it can also cause localized high heat and arcing, increasing the risk of fire.

      What to do

      Arcimoto will notify owners, and dealers will replace the traction-power harnesses free of charge.

      The recall is expected to begin March 30, 2020.

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

      Arcimoto is recalling 66 model year 2019-2020 FUV motorcycles. The traction-power harnesses large-gauge cable-lugs may be uncrimped or improperly crimpe...
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      Meijer recalls select mixed nuts

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

      Meijer is recalling 13,284 packages of mixed nuts.

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

      No illnesses are reported to date.

      The following product, sold in clear plastic 16-oz. packages under the Meijer brand label, is being recalled:

      • Fresh from Meijer - Mixed Nuts with Peanuts & Sea Salt – 16 oz., UPC – 7-1928380863-9, Sell by dates: 7-16-2020, 9-5-2020, 10-15-2020

      The recalled product was potentially sold between December 5, 2019, and March 9, 2020, in all Meijer super stores in Michigan, Ohio, Indiana, Illinois, Kentucky and Wisconsin.

      What to do

      Customers who purchased the recalled product should not consume it, but discard or return it to the nearest Meijer store for a full refund.

      Consumers with questions may contact Meijer at (800) 543-3704, 24 hours a day, seven days a week.

      Meijer is recalling 13,284 packages of mixed nuts. The product may contain Brazil Nuts, an allergen not declared on the label. No illnesses are repor...
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      Fresh 7 Baskets Limited expands fish products recall

      The products may contain egg, an allergen not declared on the label

      Fresh 7 Baskets Limited is is expanding its earlier recall of Aqua Okeano brand and Aqua Okeano / Seven Baskets brand fish products.

      The products may contain egg, an allergen not declared on the label.

      One reported reaction associated with the consumption of the recalled products has been reported.

      The following products, which were sold in Ontario and Quebec, and may have been distributed in other provinces or territories, are being recalled:

      BrandProductSizeUPCCodes
      Aqua OkeanoFish Ball with Cuttlefish200 g6 285048 270002All codes where egg is not declared on the label
      Aqua OkeanoFried Fish Ball200 g6 285048 270248All codes where egg is not declared on the label
      Aqua OkeanoHandmade Fish Cake with Vegetable300 g6 285048 270484All codes where egg is not declared on the label
      Aqua OkeanoWhite Fish Ball200 g6 285048 270316All codes where egg is not declared on the label
      Aqua Okeano / Seven BasketsFish Ball with Cuttlefish190 g6 28504 82707 9All codes where egg is not declared on the label
      Aqua Okeano / Seven BasketsFried Fish Ball180 g6 28504 82713 0All codes where egg is not declared on the label
      Aqua Okeano / Seven BasketsHandmade Fish Cake with Vegetable270 g6 28504 82751 2All codes where egg is not declared on the label
      Aqua Okeano / Seven BasketsWhite Fish Ball180 g6 28504 82711 6All codes where egg is not declared on the label

      What to do

      Customers who purchased the recalled products should not consume them, but discard or return them to the store where purchased.

      Consumers with questions may contact the company at (416) 299-9240.

      Fresh 7 Baskets Limited is is expanding its earlier recall of Aqua Okeano brand and Aqua Okeano / Seven Baskets brand fish products. The products may co...
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      RH recalls floor lamps

      The lamp’s on/off foot switch can overheat, melt or catch fire

      RH US of Corte Madera, Calif.. is recalling about 822 Camino floor lamps sold in the U.S., and Canada.

      The lamp’s on/off foot switch can overheat, melt or catch fire, posing a fire hazard.

      The firm has received six reports of the lamp’s foot switch overheating or catching fire, including five reports of minor property damage to flooring. No injuries have been reported.

      This recall involves the Camino floor lamps. The iron and antiqued nickel lamp measures about 68.5 inches high and 26 inches in diameter. It came with 12 25W flame or vintage cylinder candelabra bulbs at the top and a circular foot on/off switch on the electrical cord at the base.

      SKU number 68270175IRON, 68270500IRON, 68270734IRON, 68270734TSLV, 68270913ANCK, 68270915ANCK, 68270913IRON, or 68270915IRON is printed on a label located on the bottom of the lamp base.

      The lamps. Manufactured in China, were sold at RH galleries and RH outlets nationwide and online at www.restorationhardware.com from November 2012, through December 2019, for between $200 and $575.

      What to do

      Consumers should stop using and unplug the recalled lamp immediately and contact RH for a full refund of the purchase price. RH is contacting all known purchasers directly.

      Consumers may contact RH toll-free at (844) 623-7500 from 6 a.m. to 7 p.m. (PT) Monday through Friday and 8 a.m. to 5 p.m. (PT) Saturday and Sunday, by email at recall@rh.com, or online at www.restorationhardware.com and click on “Safety Recalls” at the bottom of the page.

      RH US of Corte Madera, Calif.. is recalling about 822 Camino floor lamps sold in the U.S., and Canada. The lamp’s on/off foot switch can overheat, melt ...
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