Drug recall D-0591-2025
Product
Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-6637-24. Case NDC: 00409-6637-14.
Reason for recall
Lack of Assurance of Sterility.
Lots and codes
Lot #: LH2671, Exp. 11/30/2026
Recall details
- Recalling firm
- PFIZER INC, New York, NY
- Quantity
- 15,750 vials
- Distribution
- U.S. Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 4, 2025
Related products
- Sodium bicarbonate – drug information
- NDC 0409-6637 Sodium Bicarbonate · Sodium Bicarbonate 84 mg/mL · Hospira, Inc.