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Recalls in December 2019

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    Whole Foods recalls 365 Everyday Value Dark Chocolate Sandwich Cremes

    The products may contain milk or coconut, allergens not declared on the label

    Whole Foods Market is recalling 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes and 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes.

    The products may contain milk or tree nuts (coconut), allergens not declared on the label.

    Two adverse reactions have been reported to date.

    The Dark Chocolate Peppermint Sandwich Cremes can be identified by the UPC 9948247605 and best by dates through May 1, 2020.

    The Dark Chocolate Caramel Sea Salt Sandwich Cremes can be identified by the UPC 9948247606 and best by dates through May 9, 2020.

    All were sold at Whole Foods Market stores nationwide. .

    What to do

    Customers who purchased the recalled products may bring a valid receipt into stores for a full refund.

    Consumers with questions may call (844) 936-8255 from hours of 7:00 a.m. – 10:00 p.m. (CST) Monday through Friday, or 8:00 a.m. – 6:00 p.m. (CST) Saturday and Sunday.

    Whole Foods Market is recalling 365 Everyday Value Dark Chocolate Peppermint Sandwich Cremes and 365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwic...
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    Forest River recalls Rockwood and Flagstaff recreational trailers

    The tire may contact the steel chassis outrigger, possibly resulting in tire failure

    Forest River is recalling nine model year 2020 Rockwood RLF8298KS and Flagstaff FLF8529RLS recreational trailers.

    Due to improper tire clearance, the tire may contact the steel chassis outrigger, possibly resulting in tire failure.

    Tire failure can cause a loss of vehicle control, increasing the risk of a crash.

    What to do

    Forest River will notify owners, and dealers will install a new outrigger to achieve the proper tire clearance, and damaged tires will be replaced free of charge.

    The recall was expected to begin December 27, 2019.

    Owners may contact Forest River customer service at (574) 642-8954. Forest River's number for this recall is 10C-1116.

    Forest River is recalling nine model year 2020 Rockwood RLF8298KS and Flagstaff FLF8529RLS recreational trailers.Due to improper tire clearance, the ti...
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    Lannett recalls Levetiracetam Oral Solution

    The product is contaminated with Bacillus subtilis

    Lannett Company is recalling two lots of Levetiracetam Oral Solution, which is used in the treatment of seizures.

    The product is contaminated with Bacillus subtilis, which could cause a severe infection in immunocompromised patients.

    Lannett has not received any reports of adverse events.

    The following product, which is packaged in bottles of 16 fluid ounces (one pint), is being recalled:

    ProductNDCLot NumberExpiration Date
    Levetiracetam Oral Solution 100mg/mL54838-548-802190A07/2021
    Levetiracetam Oral Solution 100mg/mL54838-548-802191A07/2021

    The recalled product, identified by the NDC and batch numbers provided above, was distributed to wholesalers/distributors nationwide.

    What to do

    Consumers who have the recalled product should contact their pharmacy to return it.

    Consumers with questions may call (866) 255-4983, Monday – Friday, 9:00 a.m. – 5:00 p.m. (EST).

    Lannett Company is recalling two lots of Levetiracetam Oral Solution, which is used in the treatment of seizures.The product is contaminated with Bacil...
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      Arcimoto recalls model year 2019 FUV motorcycles with software glitch

      The battery may shut down unexpectedly

      Arcimoto is recalling 18 model year 2019 FUV motorcycles.

      A software error may cause communication between inverters to time out, possibly resulting in an unexpected battery shut down.

      An unexpected battery shutdown, could cause the motorcycle to lose power immediately, increasing the risk of a crash.

      What to do

      Arcimoto will notify owners, and dealers will reprogram the inverter software/ firmware free of charge.

      The manufacturer has not yet provided a notification schedule.

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

      Arcimoto is recalling 18 model year 2019 FUV motorcycles.A software error may cause communication between inverters to time out, possibly resulting in...
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      Bosch Thermotechnology recalls Buderus boilers

      A blocked siphon can create a carbon monoxide hazard

      Bosch Thermotechnology of Watertown, Mass., is recalling about 170 Buderus GB125-35 oil-condensing boilers.

      The siphon can become blocked, leading to a delayed ignition that can damage the boiler’s exhaust system, creating a carbon monoxide hazard.

      No incidents or injuries are reported.

      This recall involves Buderus brand GB125-35 oil-condensing boilers distributed by Bosch.

      The boilers have a blue enclosure, and the GB125-35 model number is located on the data plate near the top right hand side of the boiler. The Buderus brand name is printed on the outside of the boiler’s blue enclosure. Bosch

      Thermotechnology and the model number are printed on a white label on the blue enclosure.

      The boilers, manufactured in Germany, were sold at wholesale distributors and installed by independent contractors nationwide from June 2008, through September 2012, for about $6,000.

      What to do

      Consumers should immediately contact Bosch for a free repair. Consumers who continue to use the boilers while awaiting repair should have a working carbon monoxide alarm installed outside of sleeping areas in the home.

      Consumers may contact Bosch Thermotechnology at (800) 323-1943 from 8 a.m. to 6 p.m. (ET) Monday through Thursday, and Friday from 8 a.m. to 5 p.m. (ET), by email at GB125.35Recall@us.bosch.com, or online at https://www.bosch-thermotechnology.us/us/en/residential/home/ and click on “Knowledge” at the top of the page, then “Product Approvals, Certifications & Regulatory Info” for more information.

      Bosch Thermotechnology of Watertown, Mass., is recalling about 170 Buderus GB125-35 oil-condensing boilers.The siphon can become blocked, leading to a...
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      Electrical issue prompts recall of Arcimoto FUV motorcycles

      Communication and display circuit boards may shut down

      Arcimoto is recalling 25 model year 2019 FUV motorcycles.

      A component of the display board may short circuit causing the communication and display circuit boards to shut down.

      As a result, the battery may shut down causing a sudden loss of power and increasing the risk of a crash.

      What to do

      Arcimoto will notify owners, and dealers will trim the pins of the 5V regulator, and apply a layer of protective tape free of charge.

      The manufacturer has not yet provided a notification schedule.

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

      Arcimoto is recalling 25 model year 2019 FUV motorcycles.A component of the display board may short circuit causing the communication and display circu...
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      Alli & Rose recalls Salted Egg Fish Skins

      The products were not inspected upon entry into the U.S.

      Alli & Rose of Redlands, Calif., is recalling approximately 21,930 pounds of Salted Egg Fish Skins.

      The products, imported from Thailand -- a country ineligible to export ready-to-eat Siluriformes (catfish) products to the U.S. -- were not presented for re-inspection upon being imported.

      There are no confirmed reports of adverse reactions.

      The following product, imported from October 21, 2019, through December 10, 2019, is being recalled:

      • 5.1-oz. pouches containing “THE SnakYard SALTED EGG FISH SKINS”

      The recalled product was shipped to retail locations in California, Maryland and New Jersey.

      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 Donna Chavez at (909) 748-0499.

      Alli & Rose of Redlands, Calif., is recalling approximately 21,930 pounds of Salted Egg Fish Skins.The products, imported from Thailand -- a country in...
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      Arcimoto recalls FUV motorcycles with electrical issue

      The communication and display circuit boards may shutdown

      Arcimoto is recalling 25 model year 2019 FUV motorcycles.

      A component of the display board may short circuit causing the communication and display circuit boards to shut down.

      If the communication or display board shuts down, the battery may shut down causing a sudden loss of power and increasing the risk of a crash.

      What to do

      Arcimoto will notify owners, and dealers will trim the pins of the 5V regulator and apply a layer of protective tape free of charge.

      The manufacturer has not yet provided a notification schedule.

      Owners may contact Arcimoto customer service at (541) 683

      Arcimoto is recalling 25 model year 2019 FUV motorcycles.A component of the display board may short circuit causing the communication and display circu...
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      Isuzu recalls vehicle with lug nut issue

      The lug nuts on the rear outer wheels may not have been properly tightened

      Isuzu Technical Center of America is recalling 1,926 model year 2017-2020 NPR-HDs, model year 2019-2020 NPR-XDs, NQRs, NRRs, Chevrolet 4500HDs, Chevrolet 5500HDs & Chevrolet 5500XDs, and model year 2020 Chevrolet 4500XD.

      The lug nuts on the rear outer wheels may not have been properly tightened when installed onto the rear axles.

      If not properly tightened, the lug nuts can loosen, causing the to wheel separate from the vehicle, increasing the risk of a crash.

      What to do

      Isuzu will notify owners, and dealers will inspect the rear outer wheel lug nuts and tightening or replacing them as necessary free of charge.

      The recall was expected to begin December 20, 2019.

      Owners may contact Isuzu customer service at (866) 441-9638 or Chevrolet customer service at (800) 222-1020. Isuzu's number for this recall is V1906.

      Isuzu Technical Center of America is recalling 1,926 model year 2017-2020 NPR-HDs, model year 2019-2020 NPR-XDs, NQRs, NRRs, Chevrolet 4500HDs, Chevrolet 5...
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      Glenmark Pharmaceuticals recalls Ranitidine tablets

      The medication may be contaminated with a probable cancer-causer

      Glenmark Pharmaceutical is recalling all unexpired lots of Ranitidine tablets.

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

      Glenmark has not received any reports of adverse events to date.

      The following products, used for treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease, are being recalled:

      NDCDescriptionExpiration Date Range
      684620-248-60;
      684620-248-01 and
      684620-248-05
      Ranitidine Tablets, USP 150mg12/2019 – 5/2022
      684620-249-30;
      684620-249-01 and
      684620-249-20
      Ranitidine Tablets, USP 300 mg12/2019 – 6/2022

      The 150 mg products product are packaged in bottle packs of 60’s, 100’s and 500’s; the 300 mg products are packaged in bottle packs of 30’s, 100’s and 250’s.

      What to do

      Customers who purchased the recalled products should immediately discontinue use and consult with their physician or healthcare provider about treatment options.

      Consumers may call Qualanex at (888) 504-2012, Monday – Friday, 9:00 am – 5:00 pm (EST) to arrange for product return.

      Glenmark Pharmaceutical is recalling all unexpired lots of Ranitidine tablets.The product may be contaminated with N-Nitrosodimethylamine (NDMA), a pro...
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      BCI Burke recalls Merge Playground Climbers

      A welded rung opening on the sides poses an entrapment hazard

      BCI Burke Company of Fond du Lac, Wis., is recalling about 440 Merge Playground Climbers.

      A welded rung opening on the sides of the climber poses an entrapment hazard to children.

      No incidents or injuries are reported.

      This recall involves the Burke Merge metal climbers used on playground equipment for children to climb up to access the play structure.

      “Burke” is printed on identification labels that are placed on the exterior of the play structure.

      The climbers, manufactured in the U.S., were sold through Burke sales representatives or Burke direct from November 2015, through August 2019, for about $1,460.

      What to do

      Consumers should immediately stop using the Merge Climbers and block them off from children’s use. BCI Burke is contacting all known owners directly by certified mail, and Burke representatives will inspect and replace climbers that are not compliant with the current voluntary standard for this product.

      Consumers may contact BCI Burke at (800) 356-2070 between 8 a.m. and 4 p.m. (CT) Monday through Friday or online at www.bciburke.com for more information.

      BCI Burke Company of Fond du Lac, Wis., is recalling about 440 Merge Playground Climbers.A welded rung opening on the sides of the climber poses an ent...
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      Motto International recalls male sexual enhancement products

      The products contain tadalafil not declared on the label

      Motto International Corp. is recalling all lots of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000 and Panther Platinum 30000.

      Analysis by the FDA has found the male sexual enhancement treatment drugs contain tadalafil, rendering them unapproved drugs for which safety and efficacy has not been established.

      The firm has not received any reports of adverse events.

      The recalled products are packaged in 2-, 4-, and 10-capsule blister pack cards and were sold by two Dallas, Texas, convenience stores.

      What to do

      Motto International is notifying its customers by email and arranging for replacement of recalled products, at the request of the customer. Consumers who purchased the recalled product in October, 2019, should stop consuming it and return any unused product to Motto International..

      Consumers with questions may contact Motto International at (469) 644-4398 Monday through Friday from 9 a.m. – 5 p.m. (CT) or by email at mottoic@gmail.com.

      Motto International Corp. is recalling all lots of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000 and Panther Platinum 30000.Anal...
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      Triumph recalls Speed Triple RS motorcycles

      The motorcycle may experience a missed gear or false neutral

      Triumph Motorcycles America is recalling 466 model year 2019 Speed Triple RS motorcycles.

      The Quickshifter Assembly, TSA body may contact the gear change linkage clamp assembly and interfere with gear changes, possibly resulting in a missed gear or false neutral.

      A missed gear or false neutral can lead to sudden loss of acceleration, increasing the risk of a crash.

      What to do

      Triumph will notify owners, and dealers will replace the linkage clamp assembly free of charge.

      The recall is expected to begin in December 2019.

      Owners may contact Triumph customer service at (888) 284-6288. Triumph's number for this recall is SRAN567.

      Triumph Motorcycles America is recalling 466 model year 2019 Speed Triple RS motorcycles.The Quickshifter Assembly, TSA body may contact the gear chang...
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      Canyon Creek recalls chicken soup

      The product contains wheat and soy, allergens, not declared on the label

      Canyon Creek Soup Company of Canada is recalling chicken soup sold exclusively in the U.S.

      The product contains wheat and soy, allergens, not declared on the label.

      There have been no confirmed reports of adverse reactions.

      The following refrigerated item, produced on January 21, 2019, is being recalled:

      • 16-oz. plastic containers containing “H-E-B MEAL SIMPLE BUTTER CHICKEN SOUP” with a UPC code 0 41220 79872 8 and a best by date of 2020 JAN 21.

      The recalled product, bearing Canada establishment number “#422” inside the Canada mark of inspection, was shipped to H-E-B retail stores in Texas.

      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 Canyon Creek Soup at (888) 217-1246.

      Canyon Creek Soup Company of Canada is recalling chicken soup sold exclusively in the U.S.The product contains wheat and soy, allergens, not declared o...
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      Matrix recalls Alpha motorcycle helmets

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

      Matrix Headgear is recalling 25 Alpha motorcycle helmets in all sizes.

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

      In addition, the helmet may not adequately protect the wearer in the event of a head impact in a crash.

      A helmet that does not stay secured to the head or adequately protect the wearer from an impact increases the risk of injury in the event of a crash.

      What to do

      Matrix will notify owners and provide a replacement helmet free of charge.

      The manufacturer has not yet provided a notification schedule.

      Owners may contact Matrix customer service at info@matrixhelmets.com.

      Matrix Headgear is recalling 25 Alpha motorcycle helmets in all sizes.The helmet retention system may fail, allowing the helmet to separate from the we...
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      Ducati recalls Multistrada 1260, 1260S and Pikes Peak motorcycles

      The side stand may be improperly welded

      Ducati North America is recalling 493 model year 2018 Multistrada 1260, 1260S and Pikes Peak motorcycles.

      The side stand may be improperly welded, potentially causing it to break.

      If the stand breaks the motorcycle may fall over, increasing the risk of injury.

      What to do

      Ducati will notify owners, and dealers will replace the side stand free of charge.

      The recall is expected to begin January 2, 2020.

      Owners may contact Ducati customer service at (888) 391-5446. Ducati's number for this recall is SRV-RCL-19-004.

      Ducati North America is recalling 493 model year 2018 Multistrada 1260, 1260S and Pikes Peak motorcycles.The side stand may be improperly welded, poten...
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      J. Crew recalls boys’ denim pants

      Small stones can be present in the pockets or waistband of the pants

      Crew Group of New York, N.Y., is recalling about 900 pair of Crewcuts boys’ stone washed denim pants.

      Small stones can be present in the pockets or waistband of the pants from the stone washing manufacturing process, posing aspiration or choking hazards to young children.

      The firm has received one report of stones found in the waistband extension of the pants. No injuries have been reported.

      This recall involves Crewcuts boys’ denim pants sold in sizes 2 and 3 and includes only pants that were made in Pakistan. Pants with style number J8406 and season FA 19 are included in the recall.

      A care label sewn into the side seam lists the style number and season. A label sewn into the waistband of the garment lists the size and country of origin and “Crewcuts.”

      UPC codes 099105125419 and 099105125420 are listed on the price tag attached to the pants.

      The pants were sold at J. Crew and Crewcuts stores nationwide and online at jcrew.com from July through October 2019, for about $50.

      What to do

      Consumers should immediately take the recalled pants away from children and remove the stones from pockets or internal waistband opening to eliminate the hazard.

      Consumers may contact J. Crew at (800) 261-7422 anytime, by email at 24-7@jcrew.com or online at www.jcrew.com/ and click on "Product Recall Information" at the bottom of the page.

      Crew Group of New York, N.Y., is recalling about 900 pair of Crewcuts boys’ stone washed denim pants.Small stones can be present in the pockets or wais...
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      Ruiz Food Products recalls frozen sausage breakfast burritos

      The product may be contaminated with extraneous materials

      Ruiz Food Products of Florence, S.C., is recalling approximately 55,013 pounds of frozen, not ready-to-eat breakfast burritos containing eggs, sausage and cheese.

      The product may be contaminated with extraneous materials -- specifically pieces of plastic.

      There are no confirmed reports of injuries.

      The following item, produced on October 15, 2019, is being recalled:

      • 3.38-lb. Value Pack, containing 12 individually wrapped, 4.5-oz. “EL MONTEREY Signature BURRITO EGG, SAUSAGE & CHEESE” with a “Best if Used By” date of 01/15/2021 and a lot code of 19288.

      The recalled product, bearing establishment number “EST 45694” printed on the value pack bag and the individual wrappings next to the lot code, was shipped to retail locations nationwide.

      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 the company at (800) 772-6474.

      Ruiz Food Products of Florence, S.C., is recalling approximately 55,013 pounds of frozen, not ready-to-eat breakfast burritos containing eggs, sausage and...
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      Tropical Nut and Fruit Co. recalls Truly Good Foods South of the Border mix

      The product contains soy and almonds, allergens not declared on the label

      Tropical Nut and Fruit Co. of Charlotte, N.C., is recalling its Truly Good Foods South of the Border nut mix.

      The product contains soy and almonds, allergens not declared on the label.

      No illnesses have been reported to date.

      The recalled product, Lot #29119, item # 102340, UPC # 094184110198 and best by date 04/15/2020, comes in a 25-lb. box.

      It was shipped to The Fresh Market stores in North Carolina (excluding Asheville), South Carolina (Myrtle Beach and Pawleys Island only), Virginia, Indiana, Ohio, Pennsylvania, Massachusetts, New York, Maryland, Delaware, New Jersey, Connecticut, Kentucky and Illinois.

      What to do

      Customers who purchased the recalled product should return it to the store for a full refund.

      Consumers with questions may contact Paola Chrisco at (980) 221-4356 Monday – Friday, 8am – 5pm (ET) or by email at pchrisco@tropicalfoods.com.

      Tropical Nut and Fruit Co. of Charlotte, N.C., is recalling its Truly Good Foods South of the Border nut mix.The product contains soy and almonds, alle...
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      Piaggio recalls Vespa GTV 300, GTS 300 and GTS 300 HPE scooters

      Hydrogen may be released into the brake fluid

      Piaggio Group Americas is recalling 1,328 model year 2019 Vespa GTV 300, GTS 300, and model year 2020 Vespa GTS 300 HPE scooters.

      The brake lines may have been improperly galvanized, allowing hydrogen to be released into the brake fluid.

      Hydrogen in the braking system can reduce the brake lever's ability to activate the brakes, increasing the risk of a crash.

      What to do

      Piaggio will notify owners, and dealers will install front and rear master cylinder brake flush fittings, and perform a complete brake system flush free of charge.

      The recall began November 27, 2019, and owner letters will be mailed through January 17, 2020.

      Owners may contact Piaggio customer service at (212) 380-4433. Piaggio's number for this recall is PP2ZZQ1904_GTS.

      Piaggio Group Americas is recalling 1,328 model year 2019 Vespa GTV 300, GTS 300, and model year 2020 Vespa GTS 300 HPE scooters.The brake lines may ha...
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      Daimler recalls Mercedes-Benz and Freightliner Sprinters

      The bayonet lock may be open, causing fuel leak

      Daimler Vans USA (DVUSA) is recalling 4,987 model year 2019 Mercedes-Benz and Freightliner Sprinters with diesel fuel systems.

      The bayonet lock between the fuel pump and the fuel tank may not have been closed and locked during manufacturing, resulting in a possible leak between the fuel pump and the fuel tank.

      In addition, a gas station fuel pump may not automatically stop once the tank fill level is reached, potentially causing the fuel to overflow.

      What to do

      DVUSA will notify owners, and dealers will inspect the bayonet lock on the fuel pump, locking it as necessary, free of charge.

      The recall is expected to begin December 20, 2019.

      Owners may contact DVUSA customer service at (877) 762-8267. DVUSA's number for this recall is VS3KRAFMOD.

      Daimler Vans USA (DVUSA) is recalling 4,987 model year 2019 Mercedes-Benz and Freightliner Sprinters with diesel fuel systems.The bayonet lock between...
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      Daimler Vans USA recalls Mercedes-Benz Sprinter and Freightliner vehicles

      An insufficient weld may cause seat cushions to shift

      Daimler Vans USA (DVUSA) is recalling three model year 2019 Mercedes-Benz Sprinter and Freightliner vehicles.

      A seam on the height adjuster for the front seats may have been insufficiently welded.

      The weld seam may break in a crash and cause the seat cushion to shift forward, increasing the risk of injury.

      What to do

      DVUSA will notify owners, and dealers will replace the tilt adjuster for the front seats free of charge.

      The recall is expected to begin December 20, 2019.

      Owners may contact DVUSA customer service at (877) 762-8267. DVUSA's number for this recall is VS3SITZVER.

      Daimler Vans USA (DVUSA) is recalling three model year 2019 Mercedes-Benz Sprinter and Freightliner vehicles.A seam on the height adjuster for the fron...
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      Suantianyangmei and Bingtangyangmei Waxberry recalled

      The products contain sulfites and cyclamates not declared on the label

      Lin’s Waha International of Syosset, N.Y., is recalling Suantianyangmei Waxberry and Bingtangyangmei Waxberry.

      The products contain sulfites and cyclamates not declared on the label.

      No illnesses have been reported to date.

      The recalled products, which were sold in retail stores nationwide, come in 8.11-oz. (230G) clear plastic containers.

      Suantianyangmei Waxberry has UPC code 6948576407226 and date 03.12.2020 stamped on the box. Bingtangyangmei Waxberry has UPC code 6948576407219 and date 02.13.2020 stamped on the box.

      What to do

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

      Consumers with questions may contact Selina Lin at (516) 261-9521.

      Lin’s Waha International of Syosset, N.Y., is recalling Suantianyangmei Waxberry and Bingtangyangmei Waxberry.The products contain sulfites and cyclama...
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      KZRV recalls model year 2019-2020 Connect and Sportsmen trailers

      The optional Rock Run flip up rear storage rack may detach from the trailer

      KZRV is recalling 1,122 model year 2019-2020 Connect and Sportsmen trailers equipped with an optional Rock Run flip up rear storage rack.

      The rack and all items secured to it may detach from the trailer, becoming a road hazard and increasing the risk of a crash.

      What to do

      KZRV will notify owners, and dealers will inspect and replace the mounting brackets. If the existing rack is damaged, it will be replaced with a redesigned version free of charge.

      The recall is expected to begin January 4, 2020.

      Owners may contact KZRV customer service at (800) 768-4016, extension 154 or 153. KZRV's number for this recall is KZ-2019-02.

      KZRV is recalling 1,122 model year 2019-2020 Connect and Sportsmen trailers equipped with an optional Rock Run flip up rear storage rack.The rack and a...
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      Mitsubishi recalls model year 2012-2017 i-MiEVs

      The brake vacuum pump may fail

      Mitsubishi Motors North America (MMNA) is recalling 2,108 model year 2012-2017 i-MiEVs.

      Water may penetrate the brake assist vacuum pump, causing corrosion and a failure of the brake vacuum pump.

      Without the brake vacuum pump, the driver will experience a sudden loss of braking assist, lengthening the distance needed to stop the vehicle and increasing the risk of a crash.

      What to do

      MMNA will notify owners, and dealers will replace the brake vacuum pump free of charge.

      The recall is expected to begin January 7, 2020.

      Owners may contact MMNA customer service at (888) 648-7820. MMNA's number for this recall is SR-19-002.

      Mitsubishi Motors North America (MMNA) is recalling 2,108 model year 2012-2017 i-MiEVs.Water may penetrate the brake assist vacuum pump, causing corros...
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      Keystone recalls model year 2014 Springdale trailers

      The federal ID tag may have the incorrect tire, rim and axle size

      Keystone RV Company is recalling ten model year 2014 Springdale 253FWRLLS trailers.

      The Federal Identification Tag may have the incorrect tire, rim, and axle size.

      This could lead to the unintentional overloading of the trailer, increasing the risk of a crash.

      What to do

      Keystone will notify owners, and dealers will replace the Federal Identification Tag free of charge.

      The recall was expected to begin December 2, 2019.

      Owners may contact Keystone customer service at (866) 425-4369. Keystone's number for this recall is 19-364.

      Keystone RV Company is recalling ten model year 2014 Springdale 253FWRLLS trailers.The Federal Identification Tag may have the incorrect tire, rim, and...
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      Nassau Candy Distributors recalls Nancy Adams, Dark Chocolate Graham Crackers

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

      Nassau Candy Distributors of Hicksville, N.Y, is recalling two lots of Nancy Adams, Dark Chocolate Graham Crackers.

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

      No illnesses or allergic reactions have been reported to date.

      The recalled product with UPC code 618645275860 comes in a 7.5-oz. (212g) brown paper bag with a clear window, with Best by and Best if Used by Dates of 4/30/20, 5/1/20, 5/21/20, 6/30/20, 8/4/20, stickered to the bottom of the bag.

      It was shipped to limited retailers and distributors nationwide

      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 Nassau Candy at (516) 433-7100, extensions 6130 or 7297.

      Nassau Candy Distributors of Hicksville, N.Y, is recalling two lots of Nancy Adams, Dark Chocolate Graham Crackers.The product may contain milk, an all...
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      WilliamsRDM recalls cooktop fire suppressors

      The suppressors can fail to activate and suppress fires

      WilliamsRDM of Ft. Worth, Texas, is recalling about 9,300 pairs of WilliamsRDM StoveTop FireStop Rangehood and Microhood Automatic Cooktop Fire Suppressors.

      The StoveTop FireStop (STFS) Rangehood and Microhood Automatic Cooktop Fire Suppressors can fail to activate the sealed openings that allow the suppressant powder to feed out of the canister and suppress the fire.

      The firm is aware of two fire suppressors that failed to operate during a product demonstration. No injuries have been reported.

      This recall involves StoveTop FireStop Rangehood (STFS Rangehood) and Microhood (STFS Microhood) Automatic Cooktop Fire Suppressors manufactured from November 7 – 13, 2016.

      The flame activated, dry chemical powder fire suppression devices mount over residential cooktop stoves in a vent hood or underneath a microwave.

      The STFS Rangehood fire supressors are silver-colored metal with a red label that states “StoveTop FireStop Rangehood” and a date code of 4516 is stamped into the top of the can under the magnet assembly.

      The STFS Microhood fire supressors have a white plastic housing that the canisters fit into. The date code of DEC 2022 is stamped into the ramp located on the underside of the product.

      The devices were sold as pairs.

      The fire supressors, manufactured in the U.S., were sold at HD Supply, Interline, Louisville Fire and Safety and Central Wholesalers nationwide and online at HomeDepot.com in November 2016, for about $56, for STFS Rangehood, and $80 for STFS Microhood.

      What to do

      Consumers should immediately stop using the recalled fire supressors and contact WilliamsRDM to receive free replacements.

      Consumers may contact WilliamsRDM StoveTop FireStop toll-free at (888) 616-7976 from 8 a.m. to 5 p.m. (CT) Monday through Friday, by email at stfs@stovetopfirestop.com , or online at www.stovetopfirestop.com and click on “Recall 2018” at the bottom of the page for more information.

      WilliamsRDM of Ft. Worth, Texas, is recalling about 9,300 pairs of WilliamsRDM StoveTop FireStop Rangehood and Microhood Automatic Cooktop Fire Suppressors...
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      Hodgson Mill Issues recalls Unbleached All-Purpose White Wheat Flour

      The product may be contaminated with pathogenic E. coli

      Hodgson Mill of Effingham, Ill., is recalling specific lots of its Unbleached All-Purpose White Wheat Flour.

      The product may be contaminated with pathogenic E. coli.

      There are no confirmed reports of illnesses.

      The following item, sold nationwide, is being recalled:

      • Unbleached All-Purpose White Wheat Flour (5 lb.) UPC 0-71518-05009-2 Best By Date 10-01-2020 and 10-02-2020 with lot codes listed Lot# 001042 & 005517  

      The Use By and Lot Code information can be found on the bottom back panel of the bag.

      What to do

      Customers who purchased the recalled product should not consume it, but return it to the place of purchase for a full refund.

      Consumers with questions may contact the company at (888) 417-9343. ext. 1, Monday -- Friday, 9am -- 3pm.

      Hodgson Mill of Effingham, Ill., is recalling specific lots of its Unbleached All-Purpose White Wheat Flour.The product may be contaminated with pathog...
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      Thor Motor Coach recalls Tuscany and Venetian motorhomes

      The rear reflectors within the taillight lens may not be positioned correctly

      Thor Motor Coach (TMC) is recalling 1,785 model year 2014-2017 Tuscany XTE (models 34ST, 36MQ, 40AX, 40BX, 40EX & 40GQ), model year 2013-2018 Tuscany (models 38SQ, 40DX, 40KQ, 40RX, 42GX, 42HQ, 42WX, 44MT 45AT & 45LT) and model year 2016-2020 Venetian (models A40, B42, F42, G36, J40, L40, M37, R40, S40, & T42) motorhomes.

      The rear reflectors within the taillight lens may be too high, reducing the vehicle's visibility.

      The incorrectly positioned reflectors may make the motorhome less visible to others on the road, increasing the risk of a crash.

      What to do

      TMC will notify owners, and dealers will install adhesive reflectors free of charge.

      The recall is expected to begin January 3, 2020.

      Owners may contact TMC customer service at (877) 855-2867. TMC's number for this recall is RC000180.

      Thor Motor Coach (TMC) is recalling 1,785 model year 2014-2017 Tuscany XTE (models 34ST, 36MQ, 40AX, 40BX, 40EX & 40GQ), model year 2013-2018 Tuscany (mode...
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      Winnebago recalls Itasca Vista, Sunstar and Adventurer 35F motorhomes

      An electrical connector was mounted improperly

      Winnebago Industries is recalling 638 model year 2017-2020 Itasca Vista, Sunstar and Adventurer 35F motorhomes.

      An electrical connector was mounted directly on the floor instead of to a standoff bracket as intended.

      If the floor gets wet where the electrical connection is mounted, there is an increased risk of an electrical short and fire.

      What to do

      Winnebago will notify owners, and dealers will correctly mount the electrical connector onto a metal standoff bracket free of charge.

      The manufacturer has not yet provided a notification schedule.

      Owners may contact Winnebago customer service at (641) 585-6939 or (800) 537-1885. Winnebago's number for this recall is 160.

      Winnebago Industries is recalling 638 model year 2017-2020 Itasca Vista, Sunstar and Adventurer 35F motorhomes.An electrical connector was mounted dire...
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      Aston Martin recalls DB11 Coupes, Volantes and Vantage and DBS Superleggera Coupes

      The locking nut fasteners on the passenger airbag may not be tightened properly

      Aston Martin The Americas is recalling 17 model year 2018-2019 DB11 Coupes & Volantes, and model year 2019 Vantage& DBS Superleggera Coupes.

      The locking nut fasteners on the passenger airbag may not be tightened properly.

      The airbag may not deploy properly in a crash, increasing the risk of injury.

      What to do

      Aston Martin will notify owners, and dealers will inspect the air bag fasteners, tightening them as necessary, free of charge.

      The recall is expected to begin December 18, 2019.

      Owners may contact Aston Martin customer service at (866) 278-6661. Aston Martin's number for this recall is RA-01-1327.

      Aston Martin The Americas is recalling 17 model year 2018-2019 DB11 Coupes & Volantes, and model year 2019 Vantage& DBS Superleggera Coupes.The locking...
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      Newmar recalls model year 2020 Mountain Aire motorhomes

      The low beam bulbs may malfunction

      Newmar Corporation is recalling six model year 2020 Mountain Aire motorhomes built on a Daimler Trucks North America (DTNA) chassis.

      The low beam bulbs may not remain illuminated when the high beam bulbs are activated.

      If both beams are not illuminated together as intended, the driver may have reduced visibility, increasing the risk of a crash.

      What to do

      Newmar will notify owners, and DTNA dealers will repair as necessary to ensure the low beam bulb will illuminate along with the high beam bulb free of charge.

      The recall is expected to begin January 14, 2020.

      Owners may contact Newmar customer service at (800) 731-8300 or DTNA customer service at (800) 547-0712.

      Newmar Corporation is recalling six model year 2020 Mountain Aire motorhomes built on a Daimler Trucks North America (DTNA) chassis.The low beam bulbs...
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      UNFI recalls Wild Harvest flour

      The product may be contaminated with E. coli

      UNFI is recalling five-pound bags of its Wild Harvest Organic All-Purpose Flour, Unbleached.

      The product may be contaminated with E. coli.

      There have been no direct consumer reports of confirmed illnesses.

      The following product is being recalled:

      • Wild Harvest Organic All-Purpose Flour, Unbleached, UPC 711535509158, Best if Used by Date 010820 CC 15:58 (found on top of the product)

      What to do

      Customers who purchased the recalled product should discard it.

      Consumers with questions may contact UNFI at (855) 423-2630 seven days-a-week from 8:00 AM to 8:00 PM( CST).

      UNFI is recalling five-pound bags of its Wild Harvest Organic All-Purpose Flour, Unbleached.The product may be contaminated with E. coli.There have...
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      Northern Fisheries recall tuna medallions

      The product may contain elevated levels of histamine

      Northern Fisheries LTD of Little Compton, R.I., is recalling frozen, wild-caught yellowfin Tuna Medallions – a product of Vietnam.

      The product may contain elevated levels of histamine, which can produce an allergic reaction with symptoms that include tingling or burning sensation in the mouth, facial swelling, rash, hives and itchy skin, nausea, vomiting or diarrhea.

      The symptoms usually disappear within several hours without medical intervention.

      Tuna King, sold in Connecticut, Michigan, Minnesota, Rhode Island and Wisconsin, is being recalled. Details:

      • Description: Tuna Medallions 2-3oz 10x1lb
      • Production date: 06/13/2019
      • Northern lot #: 0058797
      • UCP code: 815838020638

      The production date and UPC code are on back of the Tuna King Brand rider card.

      What to do

      Customers who purchased the recalled products should not consume them, but discard them immediately.

      Consumers with questions may contact the company at (401) 592-0600, Monday through Friday, 9 a.m. to 5 p.m. (ET) or by email at northfish@northfishltd.com.

      Northern Fisheries LTD of Little Compton, R.I., is recalling frozen, wild-caught yellowfin Tuna Medallions – a product of Vietnam.The product may conta...
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      Amneal Pharmaceuticals recalls various lots of ranitidine tablets and syrup

      The medications may be contaminated with a probable cancer-causer

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

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

      Ranitidine is a histamine-2 blocker, which decreases the amount of acid created by the stomach, and is used for treatment and prevention of ulcers of the stomach and intestines and treatment of gastroesophageal reflux disease.

      No confirmed adverse events have been directly related to the recalled products.

      Products with the following NDC numbers are being recalled:

      ProductStrengthPack SizeNDC 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, USP150 mg1000 count53746-253-10
      Ranitidine Tablets, USP300 mg30 count65162-254-03
      Ranitidine Tablets, USP300 mg100 count65162-254-10
      Ranitidine Tablets, USP300 mg250 count65162-254-25
      Ranitidine Tablets, USP300 mg250 count53746-254-02
      Ranitidine Syrup (Ranitidine Oral Solution, USP)15 mg/mL;
      6 fl. oz.
      473 mL65162-664-90

      The following lot numbers are included in the recall:  

      Ranitidine Tablets, USP, 150mg

      NDC No.DescriptionLotExpiration Date
      53746-253-10Ranitidine Tablets, USP 150mgHB03718A3/2020
      53746-253-10Ranitidine Tablets, USP 150mgHB03818A3/2020
      53746-253-10Ranitidine Tablets, USP 150mgHB03918A3/2020
      53746-253-10Ranitidine Tablets, USP 150mgHB04018A3/2020
      53746-253-10Ranitidine Tablets, USP 150mgHC01618A3/2020
      53746-253-10Ranitidine Tablets, USP 150mgHC14618A5/2020
      53746-253-10Ranitidine Tablets, USP 150mgHC14718A5/2020
      53746-253-10Ranitidine Tablets, USP 150mgHC14818A5/2020
      53746-253-10Ranitidine Tablets, USP 150mgHC14918A5/2020
      53746-253-10Ranitidine Tablets, USP 150mgHC15018A5/2020
      53746-253-10Ranitidine Tablets, USP 150mgHK02318A9/2020
      53746-253-10Ranitidine Tablets, USP 150mgHK02418A9/2020
      53746-253-10Ranitidine Tablets, USP 150mgHK02518A9/2020
      53746-253-10Ranitidine Tablets, USP 150mgHK02618A9/2020
      53746-253-10Ranitidine Tablets, USP 150mgHD03119A3/2021
      53746-253-10Ranitidine Tablets, USP 150mgHD03219A3/2021
      53746-253-10Ranitidine Tablets, USP 150mgHE03119A4/2021
      53746-253-10Ranitidine Tablets, USP 150mgHE03219A4/2021
      NDC No.DescriptionLotExpiration Date
      65162-253-06Ranitidine Tablets, USP 150mgAR171764A11/2019
      65162-253-06Ranitidine Tablets, USP 150mgAR171875A11/2019
      65162-253-06Ranitidine Tablets, USP 150mgAR171876A11/2019
      65162-253-06Ranitidine Tablets, USP 150mgAR171981A11/2019
      65162-253-06Ranitidine Tablets, USP 150mgAR180020C1/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180206A1/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180207A1/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180208A1/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180438A2/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180439A2/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180481A3/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180482A3/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR180483A3/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR181690A10/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR181691A10/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR181806A11/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR190058A12/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR190059A12/2020
      65162-253-06Ranitidine Tablets, USP 150mgAR190183A1/2021
      65162-253-06Ranitidine Tablets, USP 150mgAR190184A1/2021
      NDC No.DescriptionLotExpiration Date
      65162-253-10Ranitidine Tablets, USP 150mgAR171984A12/2019
      65162-253-10Ranitidine Tablets, USP 150mgAR180020B1/2020
      65162-253-10Ranitidine Tablets, USP 150mgAR180675A4/2020
      65162-253-10Ranitidine Tablets, USP 150mgAR180868B5/2020
      65162-253-10Ranitidine Tablets, USP 150mgAR181807A11/2020
      65162-253-10Ranitidine Tablets, USP 150mgAR190366B2/2021
      NDC No.DescriptionLotExpiration Date
      65162-253-11Ranitidine Tablets, USP 150mgAR171986A12/2019
      65162-253-11Ranitidine Tablets, USP 150mgAR171987A12/2019
      65162-253-11Ranitidine Tablets, USP 150mgAR180255A1/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180441A2/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180442A2/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180559A3/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180560A3/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180594A3/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180595A3/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180829A4/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180831A5/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180832A5/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR180868A5/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR181807C11/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR190085A12/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR190086A12/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR190087A12/2020
      65162-253-11Ranitidine Tablets, USP 150mgAR190124A1/2021
      65162-253-11Ranitidine Tablets, USP 150mgAR190542B3/2021
      65162-253-11Ranitidine Tablets, USP 150mgAR190609A3/2021
      65162-253-11Ranitidine Tablets, USP 150mgAR190610A3/2021
      NDC No.DescriptionLotExpiration Date
      65162-253-18Ranitidine Tablets, USP 150mgAR171875B11/2019
      65162-253-18Ranitidine Tablets, USP 150mgAR180483B3/2020
      65162-253-18Ranitidine Tablets, USP 150mgAR181807B11/2020
      65162-253-18Ranitidine Tablets, USP 150mgAR190008B12/2020
      NDC No.DescriptionLotExpiration Date
      65162-253-50Ranitidine Tablets, USP 150mgAR171763A11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171764B11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171874A11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171875C11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171877B11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171878B11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171982A11/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171983A12/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR171985A12/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR180016A12/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR180017A12/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR180018A12/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR180019A12/2019
      65162-253-50Ranitidine Tablets, USP 150mgAR180020A1/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180208B1/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180256A1/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180291A1/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180292A1/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180293A1/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180294A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180295A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180364A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180365A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180366A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180367A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180368A2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180440B2/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180484A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180485A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180556A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180557A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180558A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180596A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180597A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180598A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180599A3/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180675B4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180676A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180677A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180678A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180679A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180801A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180802A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180803A4/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180869A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180870A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180871A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180872A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180994A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180995A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180996A5/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180997A6/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR180998A6/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181158A7/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181159A7/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181160A7/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181161A7/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181692A10/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181693A10/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181694A10/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181709A10/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181710A11/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181711A11/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181808A11/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR181809A11/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190004A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190005A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190006A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190007A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190008A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190088A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190089A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190090A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190121A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190122A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190123A12/2020
      65162-253-50Ranitidine Tablets, USP 150mgAR190125B1/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190181A1/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190182A1/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190364A2/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190365A2/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190366A2/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190509A3/2021
      65162-253-50Ranitidine Tablets, USP 150mgAR190510A3/2021

      Ranitidine Tablets, USP, 300mg

      NDC No.DescriptionLotExpiration Date
      53746-254-02Ranitidine Tablets, USP 300mgHB04118A2/2020
      53746-254-02Ranitidine Tablets, USP 300mgHB04218A2/2020
      53746-254-02Ranitidine Tablets, USP 300mgHB04318A2/2020
      53746-254-02Ranitidine Tablets, USP 300mgHB04418A2/2020
      53746-254-02Ranitidine Tablets, USP 300mgHF13518A6/2020
      53746-254-02Ranitidine Tablets, USP 300mgHF13618A6/2020
      53746-254-02Ranitidine Tablets, USP 300mgHF13718A6/2020
      53746-254-02Ranitidine Tablets, USP 300mgHF13818A6/2020
      53746-254-02Ranitidine Tablets, USP 300mgHK02818A9/2020
      53746-254-02Ranitidine Tablets, USP 300mgHK02918A9/2020
      53746-254-02Ranitidine Tablets, USP 300mgHK03018A9/2020
      53746-254-02Ranitidine Tablets, USP 300mgHK03118A9/2020
      53746-254-02Ranitidine Tablets, USP 300mgHL08418A11/2020
      53746-254-02Ranitidine Tablets, USP 300mgHL08518A11/2020
      53746-254-02Ranitidine Tablets, USP 300mgHL08618A11/2020
      53746-254-02Ranitidine Tablets, USP 300mgHL08718A11/2020
      53746-254-02Ranitidine Tablets, USP 300mgHB01419A1/2021
      53746-254-02Ranitidine Tablets, USP 300mgHB05619A1/2021
      53746-254-02Ranitidine Tablets, USP 300mgHB05719A1/2021
      53746-254-02Ranitidine Tablets, USP 300mgHB05819A1/2021
      53746-254-02Ranitidine Tablets, USP 300mgHB05919A1/2021
      53746-254-02Ranitidine Tablets, USP 300mgHB06019A1/2021
      53746-254-02Ranitidine Tablets, USP 300mgHB06119A1/2021
      NDC No.DescriptionLotExpiration Date
      65162-254-03Ranitidine Tablets, USP 300mgAR172033B11/2019
      65162-254-03Ranitidine Tablets, USP 300mgAR180024A12/2019
      65162-254-03Ranitidine Tablets, USP 300mgAR180025A12/2019
      65162-254-03Ranitidine Tablets, USP 300mgAR180118A12/2019
      65162-254-03Ranitidine Tablets, USP 300mgAR180119A12/2019
      65162-254-03Ranitidine Tablets, USP 300mgAR180519A3/2020
      65162-254-03Ranitidine Tablets, USP 300mgAR180615A3/2020
      65162-254-03Ranitidine Tablets, USP 300mgAR181795A11/2020
      65162-254-03Ranitidine Tablets, USP 300mgAR181921B12/2020
      65162-254-03Ranitidine Tablets, USP 300mgAR190705A4/2021
      NDC No.DescriptionLotExpiration Date
      65162-254-10Ranitidine Tablets, USP 300mgAR172029A11/2019
      65162-254-10Ranitidine Tablets, USP 300mgAR172030A11/2019
      65162-254-10Ranitidine Tablets, USP 300mgAR180021A12/2019
      65162-254-10Ranitidine Tablets, USP 300mgAR180022A12/2019
      65162-254-10Ranitidine Tablets, USP 300mgAR180023A12/2019
      65162-254-10Ranitidine Tablets, USP 300mgAR180123A12/2019
      65162-254-10Ranitidine Tablets, USP 300mgAR180144A1/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180145A1/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180146A1/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180147A1/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180402A2/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180465A2/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180466A2/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180467A2/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180468A2/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR180613A3/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR181156A7/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR181157A7/2020
      65162-254-10Ranitidine Tablets, USP 300mgAR190418B2/2021
      NDC No.DescriptionLotExpiration Date
      65162-254-25Ranitidine Tablets, USP 300mgAR171800A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171801A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171802A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171803A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171804A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171931A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171932A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171933A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171934A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171935A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171936A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR171937A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172026A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172027A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172028A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172031A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172032A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172033A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172034A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR172035A11/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180030A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180031A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180032A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180033A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180034A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180113A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180114A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180115A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180117A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180120A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180121A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180122A12/2019
      65162-254-25Ranitidine Tablets, USP 300mgAR180148A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180198A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180199A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180200A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180201A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180202A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180257A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180258A1/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180335A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180336A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180337A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180338A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180339A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180374A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180375A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180376B2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180403A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180404A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180405A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180406A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180424A2/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180486A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180487A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180488A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180515A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180516A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180517A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180518A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180638A3/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180640A4/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR180641A4/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR181920A12/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR181921A12/2020
      65162-254-25Ranitidine Tablets, USP 300mgAR190414B2/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190415A2/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190416A2/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190417A2/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190418A2/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190543A3/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190544A3/2021
      65162-254-25Ranitidine Tablets, USP 300mgAR190545A3/2021

      Ranitidine Syrup (Ranitidine Oral Solution, USP)

      NDC No.DescriptionLotExpiration Date
      65162-664-90Ranitidine Syrup 15mg/mL06648001A11/2019
      65162-664-90Ranitidine Syrup 15mg/mL06648003A4/2020
      65162-664-90Ranitidine Syrup 15mg/mL06649001A1/2021

      What to do

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

      Consumers who have the recalled product should stop using it and call 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 may be contaminated with N-Nitrosodimethylamine (ND...
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      Ajinomoto Foods North America, recalls chicken fried rice

      The product may be contaminated with pieces of plastic

      Ajinomoto Foods North America of Oakland, Miss., is recalling approximately 172,692 pounds of chicken fried rice.

      The product may be contaminated with extraneous materials -- specifically pieces of plastic.

      There are no confirmed reports of adverse reactions.

      The following not-ready-to-eat, frozen item, were produced from July 9 – 11, 2019, with various packaging and best by dates, is being recalled:

      • 54-oz. cardboard packages containing “AJINOMOTO YAKITORI CHICKEN WITH JAPANESE-STYLE FRIED RICE” with date codes “3559007, 3559008, 3559015, 3559190 and 3559191” and best by dates of “1/7/2020, 1/8/2020, 1/15/2020, 7/9/2020 and 7/10/2020.”

      The recalled product, bearing establishment number “P-34708” inside the USDA mark of inspection, was shipped to retail locations in Florida, Georgia, Illinois, Maryland, Michigan, New Jersey and Texas.

      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 Willis Hwang at (855) 742-5011 or at by email at CustomerCare@ajinomotofoods.com.

      Ajinomoto Foods North America of Oakland, Miss., is recalling approximately 172,692 pounds of chicken fried rice.The product may be contaminated with e...
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      Arcimoto recalls model year 2019 FUVs

      The vehicle may lose drive power

      Arcimoto is recalling 13 model year 2019 FUVs.

      The braided shielding of the high-voltage harness may short against an energized component causing a main fuse to blow, resulting in a loss of drive power.

      A loss of power can increase the risk of a crash.

      What to do

      Arcimoto will notify owners, and dealers will inspect the harness and replace it, as necessary, free of charge.

      The manufacturer has not yet provided a notification schedule.

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

      Arcimoto is recalling 13 model year 2019 FUVs.The braided shielding of the high-voltage harness may short against an energized component causing a main...
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      Thor Motor Coach recalls Sequence 20L motorhomes

      The solar panel may detach from the luggage rack

      Thor Motor Coach (TMC) is recalling 107 model year 2020 Sequence 20L motorhomes.

      The screws securing the solar panel to the luggage rack may fail, causing the solar panel to detach.

      If the solar panel detaches from the luggage rack, it can become a road hazard, increasing the risk of a crash.

      What to do

      TMC will notify owners, and dealers will replace the screws with plates, carriage bolts, washers, and locking nuts free of charge.

      The recall is expected to begin January 3, 2020.

      Owners may contact TMC customer service at (877) 855-2867. TMC's number for this recall is RC000179.

      Thor Motor Coach (TMC) is recalling 107 model year 2020 Sequence 20L motorhomes.The screws securing the solar panel to the luggage rack may fail, causi...
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      Euroline Foods recalls Dry Fruit Mix Quince Compote

      The product contains sulfites, which are not declared on the label

      Euroline Foods of Staten Island, N.Y., is recalling DRY FRUIT MIX QUINCE COMPOTE.

      The product contains sulfites, which are not declared on the label. Those with severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume the recalled product.

      No illness or allergic reactions are reported to date.

      The recalled product, which comes in 17.65-oz. (500 gram), clear plastic package marked with container code# 27032019 and UPC code 4605932006203, was sold in retail stores and through mail orders nationwide.

      What to do

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

      Consumers with questions may contact the company at (718) 318-1888

      Euroline Foods of Staten Island, N.Y., is recalling DRY FRUIT MIX QUINCE COMPOTE.The product contains sulfites, which are not declared on the label. Th...
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      Forest River recalls Cherokee Alpha Wolf Travel Trailers

      The wire supplying power for the refrigerator may not have overcurrent protection

      Forest River is recalling 154 model year 2020 Cherokee Alpha Wolf Travel Trailers.

      The wire supplying the 12V power for the refrigerator may have been connected incorrectly to the circuit breaker.

      The incorrectly connected wire may not have overcurrent protection, allowing the wire to melt, increasing the risk of fire.

      What to do

      Forest River has notified owners, and dealers will correct the wiring free of charge.

      The recall began November 19, 2019.

      Owners may contact Forest River customer service at (260) 499-2100. Forest River's number for this recall is 76-1109.

      Forest River is recalling 154 model year 2020 Cherokee Alpha Wolf Travel Trailers.The wire supplying the 12V power for the refrigerator may have been c...
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      Precision Dose recalls Ranitidine Oral Solution

      The medication is contaminated with a probable cancer-causer

      Precision Dose is recalling five lots of Ranitidine Oral Solution.

      The product, used to treat and prevent ulcers of the stomach and intestines, and gastroesophageal reflux disease, is contaminated with N-Nitrosodimethylamine (NDMA), a probable human carcinogen, above levels established by the FDA.

      The firm has not received any reports of adverse events to date.

      The following lots of the product, USP 150 mg/10 mL packaged in unit dose cups (NDC 68094-204-59), and sold in 30-pack cartons (68094-204-62) or 100-pack cartons (68094-204-61) are being recalled:

      Lot

      Expiry

      501290

      30-Nov-2019

      501326

      30-Nov-2019

      501501

      30-Nov-2019

      501592

      30-Apr-2020

      501679

      30-Apr-2020

      The lot number and expiration date are printed on each unit dose cup and carton label.

      The recalled product was shipped nationwide to wholesalers, distributors and hospitals.

      What to do

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

      Consumers who purchased the recalled product should stop using it and call Precision Dose ( 815) 624-8523 to obtain a return packet.

      Consumers with questions may contact the firm at (815) 624-8523) Monday through Friday 8 am to 4:30 pm (CST) or by e-mail at druginfo@precisiondose.com.

      Precision Dose is recalling five lots of Ranitidine Oral Solution.The product, used to treat and prevent ulcers of the stomach and intestines, and gast...
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      Stanley Black & Decker recalls wooden handle nailing hammer

      The molded grip on the hammer can come loose

      Stanley Black & Decker of Towson, Md., is recalling about 211,000 Stanley brand 16-oz. wooden handle nailing hammers.

      The molded grip on the hammer can come loose, posing an injury hazard.

      The firm has received one report of the hammer’s grip coming loose. No injuries have been reported.

      This recall involves the STANLEY brand 16-oz. wooden handle nailing hammers with model number STHT51454 etched below the STANLEY logo on the steel hammer head.

      The hammers have a metal head, a natural wood handle with a black over- molded grip with STANLEY marked on the wooden handle in black and on the steel hammer head.

      The UPC code for the product is 076174514544 and is located on a label on the handle.

      The hammers, manufactured in Taiwan, were sold exclusively at Walmart stores nationwide from July 2018, through August 2019, for about $6.

      What to do

      Consumers should immediately stop using the recalled hammers and return them to Walmart to receive a refund in the form of a Walmart gift card for the purchase price.

      Consumers may contact Stanley toll-free at (866) 215-1132 from 8 a.m. to 5 p.m. (ET) Monday through Friday, by email at recall@sbdinc.com or online at www.stanleytools.com click on “Support” at the top of the page, then “Safety Notices and Recalls” for more information.

      Stanley Black & Decker of Towson, Md., is recalling about 211,000 Stanley brand 16-oz. wooden handle nailing hammers.The molded grip on the hammer can...
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      TMC recalls Magnitude and Omni motorhomes

      A loose seat back may not adequately restrain an occupant in a crash

      Thor Motor Coach (TMC) is recalling 229 model year 2019-2020 Magnitude and Omni motorhomes.

      The seat recliner mechanisms may be missing the third pawl required for seat back strength, resulting in a loose seat back.

      An improperly assembled recliner mechanism may have reduced strength and may not adequately restrain an occupant in a crash, increasing the risk of injury.

      What to do

      Ford has notified TMC owners, and Ford dealers will inspect the seat structures and replace them, as necessary free of charge.

      The recall began October 21, 2019.

      Owners may contact Ford customer service at (866) 436-7332 or TMC customer service at (877) 855-2867. TMC's number for this recall is RC000178.

      Thor Motor Coach (TMC) is recalling 229 model year 2019-2020 Magnitude and Omni motorhomes.The seat recliner mechanisms may be missing the third pawl r...
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      Mondelēz Global recalls Cheese Nips

      The product may contain yellow plastic pieces

      Mondelēz Global is recalling a limited quantity of Cheese Nips.

      The product may contain small food-grade yellow plastic pieces from a dough scraper.

      There are no reports of injury or illness.

      The following product, sold in the U.S., is being recalled:

      DescriptionRetail UPCBest When Used By Date
      CHEESE NIPS (11 oz. BOX)0 44000 03453 518MAY20
      19MAY20
      20MAY20

      What to do

      Customers who purchased the recalled product should not eat it, but discard it.

      Consumers with questions may contact the company at (844) 366-1171, 24 hours a day.

      Mondelēz Global is recalling a limited quantity of Cheese Nips.The product may contain small food-grade yellow plastic pieces from a dough scraper....
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      Gulf Stream recalls Amerilite, Conquest, Innsbruck, Grand River, Kingsport and Trail Master trailers

      Carbon monoxide or propane could be released into the trailer

      Gulf Stream Coach is recalling 205 model year 2020 Amerilite, Conquest, Innsbruck, Grand River, Kingsport and Trail Master trailers.

      The gas refrigerator compartment may not be properly sealed, potentially releasing carbon monoxide or flammable unburned Liquid Petroleum (LP) gases throughout the trailer, increasing the risk of fire, injury or death.

      What to do

      Gulf Stream will notify owners, and dealers will inspect the gas refrigerator for proper sealing and repair, as necessary.

      Owners may contact Gulf Stream customer service at (800) 289-8787. Gulf Stream's number for this recall is 102919.

      Gulf Stream Coach is recalling 205 model year 2020 Amerilite, Conquest, Innsbruck, Grand River, Kingsport and Trail Master trailers.The gas refrigerato...
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      Select varieties of Breakstone’s cottage cheese recalled

      The products may contain pieces of red plastic and metal

      Breakstone is recalling approximately 9,500 cases of select varieties of cottage cheese.

      The products may contain pieces of red plastic and metal.

      There have been six consumer complaints, but and no reports of illness or injury to date.

      The following products, sent to retailers and distributors in the U.S and exported to Latin America, are being recalled with a best when used by date of Dec. 10, 2019:

      SizeName of ProductPackagingIndividual Package UPC
      16ozBreakstone's 2% Milkfat Lowfat Large Curd Cottage CheesePlastic Cup, Plastic Lid, Shrink Band0 21000 30053 2
      24ozBreakstone's 4% Milkfat Large Curd Cottage CheesePlastic Cup, Plastic Lid, Shrink Band0 21000 12285 1
      24ozBreakstone's 4% Milkfat Small Curd Cottage CheesePlastic Cup, Plastic Lid, Shrink Band0 21000 12284 4

      What to do

      Customers who purchased the recalled products should not eat them, but return them to the store where purchased for an exchange or full refund.

      Consumers with questions may contact the company at (866) 572-3805 Monday through Friday, 9 a.m. to 6 p.m. (ET) for a full refund.

      Breakstone is recalling approximately 9,500 cases of select varieties of cottage cheese.The products may contain pieces of red plastic and metal.Th...
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      RESURRECTIONbeauty recalls Wintergreen Essential Oil

      The product's packaging is not child resistant

      RESURRECTIONbeauty of Holmen, Wis., is recalling about 270 packages of Wintergreen 100 Percent Pure Essential Oil.

      The product contains 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 RESURRECTIONbeauty Wintergreen Essential Oil in amber glass 0.5-fluid-ounce dropper bottles.

      The bottles have a black cap and a green label with RESURRECTIONbeauty Wintergreen 100% Pure Essential Oil printed on the front.

      The UPC code 616913145877 is printed on the back of the product

      The oil, manufactured in the U.S., was sold online at Amazon.com, Ebay.com, Etsy.com, and Resurrectionbeauty.com from December 2015, through July 2019, for about $8.

      What to do

      Consumers should immediately store the product in a safe location out of reach of children and contact RESURRECTIONbeauty for a free replacement child-resistant cap. All known purchasers are being notified directly by the firm about the recall.

      Consumers may contact RESURRECTIONbeauty collect at (608) 352-3270 from 9 a.m. to5 p.m. (CT) Monday through Friday, by email at info@resurrectionbeauty.com or online at www.resurrectionbeauty.com and click “Recall Alert” at the top of the page for more information.

      RESURRECTIONbeauty of Holmen, Wis., is recalling about 270 packages of Wintergreen 100 Percent Pure Essential Oil.The product contains methyl salicylat...
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