Class II Recall

PFIZER INC

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.
Reason
Lack of Assurance of Sterility.
Classification
Class II
Status
Ongoing
Lot
Lot #: LY3681, LY4360, LY4416, Exp. 02/28/2026
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
PFIZER INC — Class II Recall | MedicineWatch US