US Drug Recall Register
Class III · Low risk Ongoing Initiated May 14, 2026 (4 months ago)

Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradations Specifications

What was 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
NDC code
63323-696-02
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0581-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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