Fresenius Medical Care recalls 0.9% Sodium Chloride Injection due to lack of sterility assurance. Affected units have specific NDC codes and expiration dates. Consumers should stop using and contact the company for details.
Lack of Assurance of Sterility
Fresenius Medical Care is recalling certain 0.9% Sodium Chloride Injection products because they may not be sterile. This could lead to infections if used improperly. Affected products have specific NDC codes and expiration dates listed in the recall.
The injection products lack assurance of sterility, meaning they could be contaminated with bacteria or other pathogens. If used, this could lead to infections, especially in medical settings where sterile conditions are critical.
Healthcare professionals and patients who have the recalled 0.9% Sodium Chloride Injection products with the listed NDC codes and expiration dates are affected. Those using the product for medical purposes are at the highest risk.
Check the product's NDC code on the container. The affected products have specific NDC codes listed in the recall, such as 24PU06037, 24SU06001, and others, with expiration dates up to 03/31/2026.
Discard any affected products as they may not be sterile and could cause infections.
The recall includes specific NDC codes like 24PU06037, 24SU06001, and others with expiration dates up to 03/31/2026.
Check the NDC code on the product container. Affected products have specific NDC codes listed in the recall, such as 24PU06037, 24SU06001, and others with expiration dates up to 03/31/2026.
Discard the product immediately and contact Fresenius Medical Care at 1-800-323-5188 for further instructions.
We’ve drafted a message you can send Fresenius Medical Care to request your refund or repair — edit it as you like.
Subject: Recall D-0490-2025 — Fresenius Medical Care Fresenius Medical Care Hello, I own a Fresenius Medical Care that is covered by recall D-0490-2025 from Fresenius Medical Care. 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.
