Recall archive
32,164 recalls · page 465 of 1341
Reported Jan 19, 2022
Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle, Rx Only, Distributed by: TruPharma, LLC. Tampa, FL 33609;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rubicon Research Private Limited
FDA (openFDA drug enforcement)
Reported Jan 19, 2022
SOMATOM Confidence -Computed tomography systems Model 10590100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Everything Swapples, Net Wt. 11.14 OZ, UPC 8 64390 00021 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Swap Foods LLC
FDA (openFDA food enforcement)
Reported Jan 19, 2022
Clobetasol Propionate Ointment USP, 0.05%, 60g tubes, Rx only, Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taro Pharmaceuticals U.S.A., Inc.
FDA (openFDA drug enforcement)
Reported Jan 19, 2022
Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Technomed Europe
FDA (openFDA device enforcement)
Reported Jan 19, 2022
MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 19, 2022
Carbamazepine Tablets, USP 200 mg 100 Tablets Rx only NDC 13668-268-01 Manufactured by: Torrent Pharmaceuticals Ltd.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
FDA (openFDA drug enforcement)
Consumer productsReported Jan 13, 2022
Textron Specialized Vehicles Recalls Personal Transportation Vehicles (PTV), Due to Fall and Injury Hazards (Recall…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Textron Specialized Vehicles
CPSC
Reported Jan 12, 2022
Alinity m System, Part No. 08N53-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Cefixime Capsules, 400 mg, 50-count bottles, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, India,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Jan 12, 2022
Biomeme SARS-CoV-2- Real Time RT-PCR Test, Instructions for Use, Part number 100002824 Subcomponent of: SARS-CoV-2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomeme, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2022
GODAVARI brand APRICOTS, packaged in 7 oz (UPC 0 03658 50001 4) and 14 oz (UPC 0 03657 5001 5) clear plastic-film bags…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bokhary Foods, Inc.
FDA (openFDA food enforcement)
Reported Jan 12, 2022
Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flower Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Nature's Own Honey Wheat Bread, NET WT 20 oz (1LB 4 OZ) 567g, DISTRIBUTED BY FLOWERS BAKERIES, LLC THOMASVILLE, GA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flowers Foods (Corporate Offices)
FDA (openFDA food enforcement)
Consumer productsReported Jan 12, 2022
Giant Bicycle Recalls Bicycles Due to Fall and Injury Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Bicycle Inc.
CPSC
Reported Jan 12, 2022
Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Consumer productsReported Jan 12, 2022
Children's Robes Recalled by HulovoX Due to Violation of Federal Flammability Standards and Burn Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.HulovoX
CPSC
Reported Jan 12, 2022
Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Joy's Gourmet Blast Off! Bloody Mary Mix, Net Wt. 24 Oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Joy's International Foods, Incorporated
FDA (openFDA food enforcement)
Reported Jan 12, 2022
Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keurig Dr Pepper
FDA (openFDA food enforcement)
Reported Jan 12, 2022
Gatifloxacin Ophthalmic Solution, 0.5%, 2.5 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lupin Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 12, 2022
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Instructions for Use for all model numbers of the Medtronic Abre Venous Self-Expanding Stent System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
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