PFIZER INC recalls Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 600
Recalled August 27, 2025 · FDA recall D-0590-2025 · PFIZER
Hazard
Lack of Assurance of Sterility. · FDA Class II
Units
49,620 vials
Sold at
U.S. Nationwide
Description
Lack of Assurance of Sterility.
Product
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.
Manufacturer(s)
PFIZER INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →