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).
Reported: January 24, 2024 Initiated: December 21, 2023 #D-0234-2024
Product Description
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).
Reason for Recall
Presence of Particulate Matter; identified as glass
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 21200 Cartons
- Distribution
- Nationwide in the USA and Puerto Rico.
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
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).. Recalled by Pfizer Inc.. Units affected: 21200 Cartons.
Why was this product recalled? ▼
Presence of Particulate Matter; identified as glass
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 24, 2024. Severity: Critical. Recall number: D-0234-2024.
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