Pfizer recalls Heparin Sodium 2,000 units per 1,000 mL bags due to potential leakage. This may cause contamination. Check your product details to see if affected.
Lack of assurance of sterility: Bags have the potential to leak.
Pfizer is recalling Heparin Sodium 2,000 units per 1,000 mL bags because they may leak, risking contamination. This is a serious issue for medical use.
The bags may leak, which could lead to contamination of the solution. This poses a risk of infection or improper treatment during medical procedures.
Healthcare professionals and patients using this specific heparin injection product. Those with the product's lot number 5935283 are most at risk.
Check for the product name 'Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags'. Look for lot number 5935283.
Immediately stop using the recalled heparin injection product as it may leak and cause contamination.
No, the product may leak, so it should not be used. Contact Pfizer for further instructions.
The lot number is 5935283.
Check the product label for the lot number 5935283 and the specific product details mentioned in the recall notice.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0097-2023 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0097-2023 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.
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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.
