Drug Recalls
Recent drug recall reports from the FDA (US) and Health Canada, newest first. Each entry links to the full record -- product description, reason for recall, and severity classification -- refreshed daily.
WN Pharmaceuticals Ltd products
Product safety. Verify if your product is affected. If yes, stop using the recalled product. Consult your healthcare practitioner if you have used the affected …
Eugia US LLC
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
JAMP Pantoprazole Sodium
Product safety. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health con…
B. Braun Medical Inc
Presence of Particulate Matter
FDC Limited
Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Granules Consumer Health Inc.
Label mix-up: Carton incorrectly labeled.
MAIN PRODUCTS INC
Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
FDC Limited
Defective container; yellow colored spike from cap lodged in the nozzle
Luscious Eyelash & Eyebrow Growth Serum
Product safety. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health con…
SoloVital
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Supercore Products Group Inc.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Supercore Products Group Inc.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Aurobindo Pharma USA Inc
Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
Endo Pharmaceuticals, Inc.
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled as 0.125 mg instead of 0.25 mg. The blister strips inside the product carton r…
SUN PHARMACEUTICAL INDUSTRIES INC
Failed Dissolution Specifications
Hikma Pharmaceuticals USA Inc.
Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per…
Budesonide, USP
Product safety. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health con…
Novel Laboratories, Inc. d.b.a Lupin Somerset
Defective container: potential for non-sealed pouches which can lead to product leakage.
Cipla Omnigel Spray
Unauthorized product. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any heal…
Uriexo
Unauthorized product. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any heal…
Teva Pharmaceuticals USA, Inc
Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification li…
Glenmark Pharmaceuticals Inc., USA
Failed Dissolution Specifications: results below specifications
Zydus Pharmaceuticals (USA) Inc
Presence of particulate matter: glass
Suntegrity Impeccable Skin Sunscreen Foundation
Contamination. Verify if your product is affected.Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health conc…