Class II Recall

Pfizer Inc.

Product
Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intramuscular or Intravenous Use, Rx Only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-2012-03
Reason
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Classification
Class II
Status
Ongoing
Lot
Lot#: HJ3965; Exp 2024/09 Lot#: HJ8546; Exp 2024/10
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.