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.

Select B. Braun Products Recalled
April 10, 2026
On April 6, 2026, B. Braun Medical initiated a voluntary recall of specific batches of sterile water for injection, 70% dextrose injection, 0.9% sodium chloride irrigation and Lactated Ringer’s irrigation.
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Select IV Solutions Recalled
March 31, 2026
On March 17, 2026, Fresenius Kabi USA, LLC initiated a voluntary user level recall of select lots of 0.9% Sodium Chloride Injection, USP, 0.45% Sodium Chloride Injection, USP, and 5% Dextrose Injection, USP supplied in single dose freeflex® bags.
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Medical Device Correction for Omnipod 5 Pods
March 23, 2026
On March 12, 2026, Insulet Corporation initiated a voluntary medical device correction of certain Omnipod® 5 Pods.
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Ipsen Voluntarily Withdraws Tazverik
March 17, 2026
On March 9, 2026, Ipsen initiated a voluntary withdrawal of Tazverik® (tazemetostat) oral tablets from the US market, effective immediately, for all approved indications.
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Webcol Alcohol Prep Pads Recalled
March 09, 2026
On March 3, 2026, Cardinal Health issued a voluntary recall of select lots of Webcol™ Large Alcohol Prep Pads
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Udenyca Recalled
March 09, 2026
On Feb. 26, 2026, the FDA issued a class I recall for multiple lots of Accord BioPharma’s Udenyca® (pegfilgrastim cbqv) injection, 6mg/0.6mL single dose prefilled syringes.
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Urgent Correction Issued for TRUE METRIX Instructions
March 04, 2026
Summary: On Feb. 6, 2026, Trividia Health initiated an Urgent Medical Device Correction for TRUE METRIX® Blood Glucose Monitoring Systems
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One Lot of Adbry Recalled
February 25, 2026
On Feb. 12, 2026, LEO Pharma initiated a voluntary US recall of Adbry® (tralokinumab ldrm) 300 mg/2mL single dose autoinjector.
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FreeStyle Libre 3 Sensors Recalled
December 16, 2025
On Nov. 24, 2025, Abbott Diabetes Care initiated a voluntary recall of select lots of the FreeStyle Libre 3 continuous glucose monitoring sensor.
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Famotidine Recalled
November 17, 2025
On Nov. 6, 2025, Fresenius Kabi initiated a voluntary nationwide recall of three lots of famotidine injection, USP, 20mg per 2mL (10mg per mL).
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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.