Pfizer recalls 4.2% sodium bicarbonate injection (5 mEq/10mL) with glass particles that could cause injury during IV use. This product was sold in specific lots and packaging.
Presence of Particulate Matter; identified as glass
Pfizer has recalled a specific type of sodium bicarbonate injection that contains glass particles. Using this product could cause injury if particles enter the bloodstream during intravenous administration.
Glass particles in the injection can enter the bloodstream during intravenous use, potentially causing tissue damage or other complications. This occurs because the glass container may have microscopic particles that are not visible to the naked eye.
Healthcare professionals who use this injection for intravenous treatments. Patients receiving this medication under medical supervision are at risk if the product is used without proper checks.
Check for the product name '4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL)' with a glass syringe. Look for the lot number GX1542 and expiration date 01/01/2025 on the packaging.
Verify the product name, lot number (GX1542), and expiration date (01/01/2025) on the packaging.
No, this product contains glass particles that could cause injury during intravenous use. Do not use it.
Check for the product name '4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL)' with a glass syringe and lot number GX1542 with expiration 01/01/2025.
Do not use it. Contact your healthcare provider for guidance on safe alternatives.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0233-2024 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0233-2024 from Pfizer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.