Fresenius Kabi recalls 5% dextrose injection vials with potential lack of sterility. Affected units have specific NDC numbers and batch dates. Consumers should contact the company for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling 5% dextrose injection products that may not be sterile. This could lead to infections if used improperly. The recall affects specific batches and units sold in the U.S.
The product lacks assurance of sterility, meaning it could be contaminated with bacteria. If used, this might cause infections or other health issues. The risk is not specified in the recall details.
Healthcare professionals and patients using the recalled 5% dextrose injection products. Those with specific NDC numbers and batch dates are most at risk.
Check the NDC number 65219-464-05 or 65219-464-50 on the product label. Look for batch numbers 6402399, 6402400, or 6402401 with an expiration date of 02/28/2027.
Look for the NDC number 65219-464-05 or 65219-464-50 and batch numbers 6402399, 6402400, or 6402401.
5% Dextrose Injection, USP 5 g per 100 mL (50 mg per mL) 100 mL in a 100 mL freeflex bag.
Batch numbers 6402399, 6402400, and 6402401.
The expiration date is 02/28/2027.
Check the NDC number 65219-464-05 or 65219-464-50 and batch numbers 6402399, 6402400, or 6402401.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0436-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0436-2026 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.
