Pfizer Inc. recalls 8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/
See all recalls from Pfizer Inc. →Recalled Product
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).
Hazard / Issue
Presence of Particulate Matter; identified as glass
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot HA7295, EXP 03/01/2025
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for 8.4 % Sodium Bicarbonate →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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