Fresenius Kabi recalls specific thiamine HCl injections due to lack of sterility assurance. Affected lots expire through May 2026; contact for return instructions.
Lack of Assurance of Sterility
Fresenius Kabi is recalling certain thiamine HCl injections that may not be sterile. Using these products could lead to infections or other health risks if they are contaminated.
The injections lack assurance of sterility, meaning they could be contaminated with bacteria or other pathogens. This contamination could lead to infections or other health complications if the product is used.
Healthcare professionals and patients using the recalled thiamine HCl injections for medical treatment. Those most at risk are individuals with compromised immune systems or those requiring injections for specific medical conditions.
Check the product label for the lot numbers listed: C274-000047651 through C274-000049727. These lots expire between February and May 2026.
Look for the lot numbers C274-000047651 through C274-000049727 on the injection label.
No, these specific lots lack sterility assurance and could cause infections if used.
Check the product label for lot numbers C274-000047651 through C274-000049727, which expire between February and May 2026.
The recall does not specify a remedy, so contact Fresenius Kabi directly for guidance.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0335-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0335-2026 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.