FDAFDA · Food and drugs·Recall number D-0591-2025
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.
Published August 27, 2025 · Recall initiated: August 4, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM BICARBONATE
- Manufacturer
- PFIZER INC
- Distributor
- U.S. Nationwide
- Lot
- Lot #: LH2671, Exp. 11/30/2026
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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