Fresenius Kabi recalls specific batches of 0.9% Sodium Chloride Injection due to lack of sterility assurance. Affected products may cause infection if used. Check batch numbers and contact the company for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling certain batches of 0.9% Sodium Chloride Injection because they may not be sterile. Using these products could lead to infections, especially in medical settings.
The injection may not be sterile, which can lead to infections if used in medical procedures. This is a serious risk for patients undergoing treatments requiring sterile solutions.
Healthcare professionals and patients who have received the recalled batch numbers. Those using the product for medical purposes are most at risk.
Check the batch numbers listed: 6402290, 6402291, 6402411, 6402412, 6402419, 6402424, 6402425, 6402426, 6402427, 6402479, 6402480, 6402517, 6402571, 6402518. The products were sold with an expiration date of January 31, 2028 or later.
Look for the batch number on the injection bag label. The affected batches are listed in the recall notice.
Reach out to Fresenius Kabi USA, LLC for further assistance or to confirm if your product is affected.
The product may not be sterile, which can lead to infections if used in medical procedures.
Affected batch numbers include 6402290, 6402291, 6402411, 6402412, 6402419, 6402424, 6402425, 6402426, 6402427, 6402479, 6402480, 6402517, 6402571, 6402518.
Check the batch number on the injection bag label against the list provided in the recall notice.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0431-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0431-2026 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.
