Fresenius Kabi USA, LLC recalls Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696
Recalled June 17, 2026 · FDA recall D-0581-2026 · Fresenius Kabi USA
Hazard
Failed Impurities/Degradations Specifications · FDA Class III
Units
898,050 vials
Sold at
US Nationwide.
Description
Failed Impurities/Degradations Specifications
Product
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)
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →