WhichRecall
Class IIReported 2025-08-27

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.

Recalled by PFIZER INC

Reason for Recall

Lack of Assurance of Sterility.

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Recall Number
D-0590-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-08-04
Reported
2025-08-27
Distribution
U.S. Nationwide
Code Info
Lot #: LY3681, LY4360, LY4416, Exp. 02/28/2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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