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FDAFDA · Food and drugs·Recall number D-0581-2026

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)

Published June 17, 2026 · Recall initiated: May 14, 2026

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Failed Impurities/Degradations Specifications

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
EPINEPHRINE
Manufacturer
Fresenius Kabi USA, LLC
Distributor
US Nationwide.
UPC
0363323696023
Lot
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.
Risk classification
Class III
Area (FDA)
drug
Country
United States

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