FDAFDA · Food and drugs·Recall number D-0590-2025
Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045, USA. NDC 0409-4933-05. Case: NDC 0409-4933-10.
Published August 27, 2025 · Recall initiated: August 4, 2025
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
Lack of Assurance of Sterility.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- PFIZER INC
- Distributor
- U.S. Nationwide
- Lot
- Lot #: LY3681, LY4360, LY4416, Exp. 02/28/2026
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.