Fresenius Kabi recalls 500mL 0.9% Sodium Chloride Injection due to lack of sterility assurance. Affected batches expire 09/30/2027 and 10/31/2027. Consumers should contact manufacturer for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling 500mL 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 October 2027.
The products lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If used without proper sterilization, this could cause infections in patients. The risk is significant for medical use where sterility is critical.
Healthcare professionals and patients who have received the recalled 500mL 0.9% Sodium Chloride Injection products. Those using the products for medical treatments are most at risk.
Check for batch numbers 24LU10013, 24LU10014 (expiring 09/30/2027) or 24NU10001, 24NU10002 (expiring 10/31/2027) on the product label. The product is a 500mL freeflex bag labeled as 0.9% Sodium Chloride Injection, USP, Rx only.
Look for batch numbers 24LU10013, 24LU10014 (expiring 09/30/2027) or 24NU10001, 24NU10002 (expiring 10/31/2027) on the product label.
Fresenius Kabi is recalling 500mL 0.9% Sodium Chloride Injection products that lack assurance of sterility, which could lead to infections if used improperly.
Batches 24LU10013, 24LU10014 (expiring 09/30/2027) and 24NU10001, 24NU10002 (expiring 10/31/2027).
The official recall notice does not specify a replacement or remedy for this product.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0428-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0428-2026 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.
