FDA Drug Recalls

Distributor RFR, LLC. has issued a voluntary nationwide recall of Sangter Energy Supplement. The product has lot #48656, Exp. 01/2025 is packed as 3000mg 7-count blister packs within a carton for a consumer level. The product is being recalled because it contains undeclared sildenafil. Sildenafil is an active ingredient in an FDA-approved prescription drug for erectile […]

Loud Muscle Science LLC has started a voluntary recall of Launch Sequence capsules in the United States and Canada. The product contains tadalafil, which is an undeclared ingredient in the dietary supplement. Tadalafil is an FDA-approved phosphodiesterase type 5 inhibitor used to treat erectile dysfunction. It is not approved for use in dietary supplements by

Golden State Medical Supply has issued a voluntary nationwide recall of two (2) lots of Atenolol Tablets USP, 25 mg, and Clopidogrel Tablets USP, 75 mg. This is due to a labeling mix-up where the bottles labeled as containing Atenolol Tablets actually contain Clopidogrel tablets and vice versa. The recall affects only products with lot

Proper Trade LLC/My Stellar Lifestyle voluntarily recalls Wonder Pill capsules, packaged 10-count blisters co-packaged in a carton, and 60-count bottles at the consumer level.  Lot 20210912 and lot 31853-501, expiry 09/24 Wonder Pill capsules, contain undeclared Tadalafil. Tadalafil is a phosphodiesterase type 5 inhibitor indicated for the treatment of erectile dysfunction and the signs and

Hospira Inc., which is a Pfizer company, voluntarily initiated a nationwide recall on August 22, 2022, of one lot of Propofol Injectable Emulsion (containing benzyl alcohol), 100mL Single Patient Use Glass Fliptop Vial; lot EA7470, because they might contain particulates. Hospira initiated this user-level recall after an annual examination of retention samples which showed the

Eugia US LLC puts a voluntary recall on Acyclovir Sodium Injection 500 mg per lot number AC22006 due to the presence of particulates. This recall is being made with the knowledge of the U.S. Food and Drug Administration (FDA). The recall is in response to complaints of the presence of dark red, brown, and/or black