Fresenius Kabi recalls 1,000mL 0.9% Sodium Chloride Injection due to lack of sterility assurance. This may cause infections if used improperly. Contact for return instructions.
Lack of Assurance of Sterility
Fresenius Kabi is recalling 1,000mL 0.9% Sodium Chloride Injection (single-dose freeflex bags) because they lack sterility assurance. Using this product could lead to infections if it's not properly sterilized.
The product lacks assurance of sterility, meaning it could be contaminated with bacteria. If used without proper sterilization, this could lead to infections in patients.
Healthcare professionals and patients who have received this specific injection product. Those using it for medical purposes are most at risk.
Look for the product name: 0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL), 1,000 mL in a Single Dose freeflex bag. Check the batch number 24EU10010 and expiration date 05/31/2027.
Verify the batch number 24EU10010 and expiration date 05/31/2027 on the product label.
No, this product lacks sterility assurance and could cause infections if used improperly.
Look for the batch number 24EU10010 and expiration date 05/31/2027 on the product label.
The recall does not specify a remedy, so contact Fresenius Kabi for further instructions.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0434-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0434-2026 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.
