8.4 % Sodium Bicarbonate Injection recall: Particulate Matter
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…
Why was 8.4 % Sodium Bicarbonate Injection recalled?
Presence of Particulate Matter; identified as glass
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot HA7295, EXP 03/01/2025
- 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…
- Recalling firm
- Pfizer Inc.
- Quantity
- 21200 Cartons
- Distribution
- Nationwide in the USA and Puerto Rico.
- Recall date
- January 24, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)