FDAFDA · Food and drugs·Recall number D-0234-2024
8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).
Published January 24, 2024 · Recall initiated: December 21, 2023
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
Presence of Particulate Matter; identified as glass
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM BICARBONATE
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide in the USA and Puerto Rico.
- Lot
- Lot HA7295, EXP 03/01/2025
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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