FDA Drug Recalls

Mylan Institutional LLC, a Viatris Company, has issued a voluntary recall of one lot of its Octreotide Acetate Injection AJ21002, exp 3/2024 due to the presence of glass particulates in the syringe. The 500 mcg/mL strength is packed in a carton containing ten 1ml syringes and was distributed nationwide in the U.S. to wholesalers/distributors (including […]

Aurobindo Pharma USA, Inc. is voluntarily recalling two (2) lots of Quinapril Hydrochlorothiazide Tablets USP, 20 mg/12.5 mg to the patient/consumer level. These lots are being recalled because they have been found to contain trace amounts of an unexpected impurity called N-nitroso quinapril, during a routine stability test. The presence of Nitrosamine Drug Substance Related

Family Dollar has voluntarily recalled certain over-the-counter products regulated by the FDA over concerns about storage outside of labeled temperature requirements. The products were stored and distributed to certain stores on or around May 1, 2022, through June 10, 2022. Family Dollar has not received any reports of adverse effects related to the consumption of

Hospira, Inc., a Pfizer company is issuing a voluntary nationwide recall of one lot of Propofol Injectable Emulsion, USP (Containing Benzyl Alcohol). The affected product is a 100 mL Single Patient Use Glass Fliptop Vial, Lot DX9067. The user-level recall is being conducted due to the potential for the presence of visible particulate matter in

Exela Pharma Sciences, LLC, (Exela) has issued a voluntary nationwide recall of Sodium Bicarbonate Injection, USP 8.4%, 50 mEq/50 mL vial, 20 count cartons due to a small number of reports of vial breakage during shipping and handling. Risk Statement Vial breakage and flying glass poppers pose serious risks, which may result in injury to healthcare

Smyrna, TN, Vi-Jon, LLC expands its voluntary recall of all flavors and lots within the expiry of magnesium citrate saline laxative oral solution because of microbial contamination. The recall affects the Magnesium Citrate Saline Laxative Oral Solution of Cherry Flavor and Grape Flavor. The affected products are 10 FL OZ (296 mL) within expiry. The