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FDA Lists Nine Eye-Care Products in Recall Over Sterility Concerns

The manufacturer initiated the action that the FDA classified as Class II, prompting consumers to check lot numbers and stop using matched products.

Houston Compounder Recalls Injectable Wellness Products Over Endotoxin Contamination

Spanish Regulator Orders Withdrawal of FluorKin Children’s Mouthwash Over Bacterial Find

Vitruvias Recalls Lot of Thyroid Tablets Over 'Superpotent' Test Results

Nearly 40,000 Clear Eyes Bottles Recalled Over Sterility Concerns

ANMAT Prohibits Specific Lots of Átomo Desinflamante and Zetrotrax After Theft

Nearly 12 Million Rohto Eye Drop Cartons Recalled Over Sterility Concerns

Major Rugby Recalls 12 Batches of Levothyroxine Nationwide

Anvisa Says Retatrutida Is Unapproved as Illegal Versions Spread

Manufacturer Recalls Generic Zyrtec Over Possible Ranitidine Contamination

Peru Orders Recall and Destruction of Premier Facial Cleanser After Bacterial Contamination

More Than 2.5 Million Lupin Eye Drop Bottles Recalled Nationwide

FDA Adds Bemotrizinol to U.S. Sunscreen Ingredients, First New Filter in Over 20 Years

Haleon Recalls Four Lots of Gas‑X Extra Strength Softgels

Anvisa Suspends Enalapril and Halaven Lots After Manufacturers Report Quality and Labeling Faults

Pharmacal Recalls One Lot of MG217 Eczema Cream Over Staph Contamination

Nalpac Recalls DTF Sexual Chocolate for Undeclared Viagra and Cialis Ingredients

FDA Flags Recall of 3.1 Million Store-Brand Eye Drops Over Sterility Concerns

3.1 Million Bottles of Store-Brand Eye Drops Recalled for Sterility Concerns

UK Regulator Recalls 50,000 Hibiwash Bottles Over Bacterial Contamination Risk