Fresenius Kabi recalls 1000mL 0.9% Sodium Chloride Injection due to lack of sterility assurance. Affected batches expire through 2028. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling 1000mL 0.9% Sodium Chloride Injection products that may not be sterile. This could lead to infections if used improperly. The recall affects specific batches with expiration dates through 2028.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. If used, this could cause infections or other health issues. The risk is particularly concerning for medical procedures where sterile conditions are critical.
Healthcare professionals and patients using the recalled injection products. Those with the specific batch numbers listed in the recall are most at risk.
Check the batch number on the product label. The recalled items include specific batches with expiration dates through 2028, such as 23SU10001 (expiring 12/31/2026) and 24AU10003-24AU10005 (expiring 01/31/2027).
Look for the batch number on the product label to determine if it is in the recalled list.
Reach out to Fresenius Kabi USA, LLC for further instructions on the recall.
The product lacks assurance of sterility, which means it could contain harmful bacteria or contaminants.
The affected batches include 23SU10001 (expiring 12/31/2026), 24AU10003-24AU10005 (expiring 01/31/2027), 24EU10001-24EU10002 (expiring 05/31/2027), 24PU10002 (expiring 11/30/2027), 25BU10003 (expiring 02/29/2028), and 25EU10005 (expiring 05/31/2028).
Check the batch number on the product label. The recalled items have specific batch numbers with expiration dates through 2028.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0433-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0433-2026 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.
