Recall Notices

After notification of any recall, Express Scripts will continue processing new and refill prescriptions with product from non-recalled lots or manufacturers, if available. Please visit the U.S. Food and Drug Administration (FDA) website for the most up-to-date information on drug safety and recalls.

Sodium Chloride Injection Recalled
August 28, 2026
Baxter International Inc. announced on Aug. 25, 2026, a voluntary nationwide recall of 0.9% Sodium Chloride Injection 500mL VIAFLEX Plastic Container.
Thyroid Tablets Recalled
August 28, 2026
On Aug. 21, 2026, Vitruvias Therapeutics, Inc. initiated a voluntary recall for one lot of Thyroid Tablets, USP 30mg.
Yimmugo Lots Withdrawn
August 28, 2026
Biotest AG initiated a voluntary withdrawal for certain lots of Yimmugo® (immune globulin IV, human-dira), 10% liquid, on Aug. 13, 2026.
Gamunex Recalled
August 21, 2026
On Aug. 12, 2026, Grifols Therapeutics initiated a voluntary withdrawal of one lot of Gamunex®-C (immune globulin injection [human], 10%), 40g/400mL vial.
Gammaked Recalled
August 21, 2026
On Aug. 11, 2026, Grifols Therapeutics initiated a voluntary withdrawal of one lot of Gammaked™ (immune globulin injection [human], 10%), 20g.
Tyenne Recalled
August 21, 2026
On Aug. 10, 2026, Fresenius Kabi initiated a voluntary recall of Tyenne® (tocilizumab-aazg) Injection, 400mg/20mL (20mg/mL), 20mL vials.
Various Baxter Healthcare Products Recalled
August 19, 2026
On Aug. 7, 2026, Baxter Healthcare Corporation initiated a voluntary recall of selected lots of Myxredlin® (insulin human), Cardene IV® (nicardipine hydrochloride), Nexterone® (amiodarone HCl), and multiple injectable famotidine, clindamycin, dexmedetomidine, vasopressin, vancomycin, pantoprazole, and daptomycin products
Morphine Sulfate Injection Recalled
August 19, 2026
On Aug. 4, 2026, Fresenius Kabi initiated a nationwide voluntary recall of one lot of Morphine Sulfate Injection
Withdrawal of Alyglo Lots
August 19, 2026
On July 30, 2026, GC Biopharma Corporation initiated a voluntary market withdrawal for three lots of Alyglo® (immune globulin intravenous, human-stwk) 10% Liquid.
Cefazolin Recalled
August 13, 2026
On July 24, 2026, Baxter International Inc. initiated a voluntary recall of cefazolin in dextrose injection, USP, 2g/100mL (20mg/mL), single-dose infusion bag, 100mL.

The information on this site is not intended to take the place of your doctor or other healthcare professionals. It is a resource to help you make the best decisions and get the most from the medical services available to you. A licensed physician should be consulted for diagnosis and treatment of all medical conditions.