Fresenius Kabi recalls 50mL 0.9% Sodium Chloride Injection (Rx only) due to lack of sterility assurance. Products with specific batch numbers and expiration dates are affected. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling 50mL 0.9% Sodium Chloride Injection (Rx only) because it may not be sterile. This could lead to infections if used improperly. The recall affects specific batch numbers and expiration dates.
The product may not be sterile, which could cause infections if used in medical procedures. This is a serious risk for patients receiving injections.
Patients prescribed this injection by a healthcare provider. Those using the product without medical supervision are not affected.
Check the product label for batch numbers 6402372, 6402374 (expiring 08/31/2026) or 6402437 (expiring 10/31/2026). The product is a 50mL 0.9% Sodium Chloride Injection for prescription use only.
Look for batch numbers 6402372, 6402374 (expiring 08/31/2026) or 6402437 (expiring 10/31/2026) on the label.
The product may not be sterile, which could cause infections. Do not use without confirming it's not recalled.
Contact Fresenius Kabi directly for instructions on what to do with the product.
Check the label for batch numbers 6402372, 6402374 (expiring 08/31/2026) or 6402437 (expiring 10/31/2026).
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0425-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0425-2026 from Fresenius Kabi. 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.
