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Latest recalls
34,959 found- Stop using nowConsumer product
JumpSport Recalls Mini Trampolines Due to Injury Hazard; New Instructions and Warning Labels Provided
JumpSport recalls half-fold mini trampolines due to risk of frame injury. Consumers must stop using and download new safety instructions from JumpSport's website.
JumpSportFeb 26, 2019 - Use cautionConsumer product
D&D Futon Furniture Recalls Sleeper Chair Folding Foam Beds Due to Violation of Federal Mattress Flammability Standard
Recall of gray Sleeper Chair Folding Foam Beds sold in 24-48" widths due to fire hazard from failing federal flammability standards. Consumers must stop using and get free fitted liners.
D&D Futon FurnitureFeb 26, 2019 - Use cautionMeat & poultry
Russ Davis Wholesale - Crazy-Fresh Recalls Chicken Products due to Misbranding and Undeclared Allergens
USDA FSIS recalls 702 lbs of chicken Caesar salad products from Feb 2019 due to undeclared milk and anchovies, allergens not listed on labels. Consumers urged to stop using these products.
Russ Davis Wholesale Crazy-FreshFeb 25, 2019 - Lower riskMedical device
Nidek, Inc. recalls NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image
Nidek recalls CEM-530 Specular Microscopes with serial numbers 120080-120096 and 170001 due to electromagnetic noise exceeding safety standards. Affected users should contact Nidek for details.
NidekFeb 25, 2019 - Lower riskMedical device
Cook Medical Incorporated recalls Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach, Catalog Number IGTCFS-65-1-UNl-C
Cook Medical recalls certain vena cava filter sets for femoral and jugular vein approaches due to updated instructions for use. This recall does not involve a safety hazard but requires users to review the latest instructions to ensure proper application.
Cook MedicalFeb 25, 2019 - Use cautionDrug
Macleods Pharma Usa Inc recalls Telmisartan and Hyrdochlorothiazide Tablets 80 mg/25 mg, 30-count bottles, Rx Only, Manufactured for: Macleods Pharma
Macleods Pharma USA recalls specific lots of Telmisartan and Hydrochlorothiazide tablets because they failed content uniformity specifications.
Macleods PharmaFeb 25, 2019 - Stop using nowFood
Schiff Foods Products recalls Schiff Food, Jalapeno Powder, 50 lb. box
Schiff Foods Products recalls 50 lb boxes of Jalapeno Powder (Lot 6490I) due to Salmonella contamination. Check your pantry for this specific lot.
Schiff FoodsFeb 25, 2019 - Lower riskFood
Albertsons Companies LLC recalls Signature Caf¿ Tomato Basil Bisque Soup: polypropylene cups with linear low density polyethylene caps, and with plastic
Albertsons recalls Signature Tomato Basil Bisque Soup due to a misplaced temperature data logger in retail packaging, which could affect cooling safety.
AlbertsonsFeb 25, 2019 - Stop using nowFood
Utz Quality Food Inc recalls Bachman Original Twist Pretzels,10 oz.Bag (flexible film) UPC: 0-77817-10580-8
Utz Quality Food recalls Bachman Original Twist Pretzels due to undeclared milk. Check your pantry if you bought these in CT, DE, MA, MD, ME, NC, NH, NJ, NY, PA, RI, VT, or WV.
BachmanFeb 25, 2019 - Lower riskFood
JOY GOURMET FOODS LLC recalls JOY GOL-GAPPA (PANI PURI) MASALA CONCENTRATE, NET WT 8 OZ (228g), UPC: 6 80617 60414 5
Joy Gourmet Foods LLC recalls 8oz panir puri masala concentrate (UPC 680617604145) for undeclared sulfites. Consumers should check labels and contact the company for details.
Joy GourmetFeb 25, 2019 - Use cautionMeat & poultry
Bellisio Foods Recalls Boneless Pork Rib Frozen Entrée Products Due to Possible Foreign Matter Contamination
USDA FSIS recalls 173,376 pounds of frozen pork rib entrées from Bellisio Foods that may contain glass or hard plastic pieces. Consumers are urged not to consume these products and should discard or return them.
Bellisio FoodsFeb 23, 2019 - Lower riskMeat & poultry
TV Food LLC. Recalls Siluriformes Products Produced Without Benefit of Inspection
TV Food LLC recalls 27,956 pounds of frozen catfish products that were not re-inspected for U.S. import compliance. Consumers are urged not to consume these items and should discard or return them.
TV Food LLCFeb 22, 2019 - Lower riskMeat & poultry
Fulton Seafood Inc. Recalls Siluriformes Products Produced Without Benefit of Inspection
Fulton Seafood recalls 100,924 pounds of wild-caught catfish produced without federal inspection. Consumers are urged not to consume these products and should dispose of or return them.
Fulton SeafoodFeb 22, 2019 - Use cautionVehicle
KIA SOUL (2016) recall — Engine
Kia is recalling 2012-2016 Soul vehicles with 1.6L GDI engines due to potential engine stall, piston damage, and fire risks from leaking oil. Owners must contact Kia for free repairs.
KiaFeb 22, 2019 - Use cautionVehicle
MERCEDES-BENZ SPRINTER (VS30) (2019) recall — Exterior Lighting
Daimler Vans USA recalls 2019 Mercedes-Benz Sprinter VS30 vehicles with non-functioning rear fog lamps, which may increase crash risk due to reduced visibility. Owners must contact DVUSA for free software update.
Mercedes-BenzFeb 22, 2019 - Lower riskMedical device
Luminex Molecular Diagnostics recalls xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple
Luminex recalls xTAG Gastrointestinal Pathogen Panel kits with lower MS2 MFI values. Affected lots expire by 12/31/2018 and 4/30/2019. No remedy specified in recall notice.
LuminexFeb 22, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Integrated ECG cable with 3-lead leadwires labeled as the following: 1. ECG TRUNK CABLE, 3-LD W/ INTEGRATED GRABBER
GE Healthcare recalls ECG cables with 3-lead leadwires that may short circuit during defibrillation, conducting 25% of defibrillation energy away from patients. Affected units include specific catalog numbers and GTINs.
GE HealthcareFeb 22, 2019 - Lower riskMedical device
Keystone Dental Inc recalls Paltop Premium Surgical Kit-containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic
Keystone Dental recalls Paltop Premium Surgical Kits with 1.25mm Hex Driver that may have oversized features causing difficulty engaging screws. Affected kits include specific part numbers and lot numbers for dental procedures.
Keystone DentalFeb 22, 2019 - Lower riskDrug
Ascend Laboratories LLC recalls Tamsulosin Hydrochloride Capsules, USP, 0.4 mg, 500-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd.,
Ascend Laboratories recalls 0.4 mg Tamsulosin capsules (NDC 67877-450-05) manufactured by Alkem Labs in India. The capsules failed dissolution tests during stability testing.
Ascend LaboratoriesFeb 22, 2019 - Use cautionDrug
Akorn, Inc. recalls Gentamicin Sulfate Ophthalmic Solution, USP, 0.3%, 5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL
Akorn recalls Gentamicin Sulfate Ophthalmic Solution (0.3%, 5mL) due to impurities detected at 18 months stability testing. This may cause eye injury if used improperly.
AkornFeb 22, 2019 - Stop using nowDrug
Golean Detox US recalls Golean DETOX capsules, 14 Net: 56 g, 14 packets containing 2 capsules per packet, 28-count capsules per box, MAT XI S.G
FDA recalls Golean Detox capsules due to undeclared sibutramine and phenolphthalein, unapproved drugs with safety concerns. Consumers should stop using if they have the product.
Golean DetoxFeb 22, 2019 - Lower riskFood
Asia Food Distributor recalls Nova Salted Biscuit The product comes in a 14.08 ounce, paper box marked with manufacturing date of Apr 2018 and
Asia Food Distributor recalls Nova Salted Biscuit due to undeclared milk content. Products manufactured April 2018 with expiration June 2020 are affected.
Asia Food DistributorFeb 22, 2019 - Lower riskMeat & poultry
J Bar B Foods Recalls Ready-To-Eat Smoked Sausage Products due to Misbranding and Undeclared Allergens
USDA recalls 51,188 pounds of ready-to-eat cheddar smoked sausage due to undeclared milk allergen and mislabeling. Consumers urged not to consume and dispose of products.
J Bar B FoodsFeb 21, 2019 - Use cautionVehicle
FORD TRANSIT (2018) recall — Power Train
XL Hybrids is recalling certain 2015-2018 Ford Transit vehicles with electric hybrid systems due to potential front driveshaft detachment causing loss of power and crash risk.
XL HybridsFeb 21, 2019 - Use cautionVehicle
PORSCHE CAYENNE (2019) recall — Visibility
Porsche recalls 2019 Cayenne models with rearview camera display software issues that may delay image response, increasing crash risk. Owners must contact Porsche for free software update.
PorscheFeb 21, 2019 - Use cautionVehicle
MACK ANTHEM (AN) (2019) recall — Service Brakes, Air
Mack is recalling certain 2018-2019 Anthem trucks with air brakes that may not stop properly during repeated braking, risking crashes. Owners must have a free air tank added by dealers.
MackFeb 21, 2019 - Use cautionVehicle
CADILLAC CT6 (2019) recall — Exterior Lighting
General Motors recalls 2019 Cadillac CT6 vehicles with turn signals that don't automatically deactivate, risking crashes due to miscommunication with pedestrians and other drivers.
CadillacFeb 21, 2019 - Lower riskMedical device
Becton Dickinson & Co. recalls BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD Synapsys is a laboratory software solution
Becton Dickinson recalls BD Synapsys software version 2.1 due to potential incorrect test order associations with culture records. Affected users should check their software version and contact support for details.
Becton DickinsonFeb 21, 2019 - Lower riskMedical device
ICU Medical, Inc. recalls icumedical ChemoLock Closed Vial Spike w/Skirt, (a) REF CL-80S-4 (4 units) (b) REF CL-80S-5 (5 units). Used in IV
ICU Medical recalls 9 units of ChemoLock Closed Vial Spikes with potential plastic burr particulate from protective caps. Stop using if you have specific lot numbers listed.
ICU MedicalFeb 21, 2019 - Use cautionMedical device
ArthroCare Corporation recalls Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971
Smith&Nephew recalls SmartStitch PerfectPasser Connector (REF # OM-8010) due to manufacturing error causing upper jaw to potentially disengage during use. Affected units have specific batch numbers.
Smith&NephewFeb 21, 2019
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