United StatesEpinephrine Injection, USP 1 mg/mL, 1 mL single‑dose vial (prescription), made by Fresenius Kabi, NDC 63323-696-02 (vial) and NDC 63323-696-25 (carton), batches 6133313, 6133314 (exp 06/2026); 6133315 (exp 07/2026); 6133682 (exp 09/2026); 6134812, 6134813 (exp 04/2027) sold nationwide in the United States is affected. The product was recalled because it failed impurities/degradations specifications.
What's being recalled
Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696-02 (vial), NDC 63323-696-25 (carton)
Recalling firm: Fresenius Kabi USA, LLC, Lake Zurich, IL, United States.
How to identify it
Batch # 6133313, 6133314, Exp Date: 06/2026; Batch # 6133315, Exp Date: 07/2026; Batch # 6133682, Exp Date: 09/2026; Batch # 6134812, 6134813, Exp Date: 04/2027.
The hazard
Failed Impurities/Degradations Specifications
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)