Fresenius Kabi recalls certain 0.9% sodium chloride injection bags due to lack of sterility assurance. This could lead to infections if used improperly. Check batch numbers and contact the company for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling specific batches of 0.9% sodium chloride injection bags because they may not be sterile. Using these bags could lead to infections, especially in medical settings where sterile solutions are critical.
The injection bags may not be sterile, which could lead to infections if used in medical procedures. This is a risk in environments where sterile solutions are essential for patient safety.
Healthcare professionals and patients who use these specific injection bags for medical treatments. Those with the listed batch numbers are most at risk.
Check the batch numbers listed: 6402153 (exp 11/30/2026), 6402297-6402298 (exp 01/31/2027), 6402377-6402379 (exp 02/28/2027), and others as detailed in the recall notice.
Look for the batch numbers listed in the recall: 6402153, 6402297, 6402298, 6402377, 6402378, 6402379, and others.
0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 100 mL in a Single Dose freeflex bag, Rx only.
Batch numbers 6402153 (exp 11/30/2026), 6402297-6402298 (exp 01/31/2027), 6402377-6402379 (exp 02/28/2027), and others as listed in the recall.
Check the batch number on the bag and compare it to 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-0430-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0430-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.