Class II
Ongoing
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.
- Company
- Pfizer Inc.
- Recall Initiated
- August 4, 2025
- Posted
- August 27, 2025
- Recall Number
- D-0591-2025
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 15,750 vials
- Firm Location
- New York, NY, United States
Reason for Recall
Lack of Assurance of Sterility.
Distribution
U.S. Nationwide
Lot / Code Info
Lot #: LH2671, Exp. 11/30/2026
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