Fresenius Kabi recalls thiamine injections due to cGMP violations. Affected lots from Canton, MA. No remedy stated in official notice.
cGMP violations
Fresenius Kabi is recalling thiamine HCl injections that were made under cGMP violations. This means the product may not meet quality standards, but the recall does not specify a fix or return process.
The product was made under cGMP violations, which are quality control standards for pharmaceuticals. This could mean the injection may not be safe or effective, but the recall does not specify how this affects patient safety.
Healthcare providers who use these injections for medical treatment. Patients receiving the product under a prescription are at risk if they use the recalled batch.
Check the product label for the NDC number 71506-079-56 and lot numbers C274-000037436 (exp. 30-Oct-24) or C274-000038893 (exp. 7-Jan-25).
Look for the NDC number 71506-079-56 and lot numbers C274-000037436 or C274-000038893 on the injection packaging.
The official recall notice does not state any remedy or fix for the product.
Check the product label for the NDC number 71506-079-56 and lot numbers C274-000037436 (exp. 30-Oct-24) or C274-000038893 (exp. 7-Jan-25).
The official recall notice does not specify any action to take for the 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-0023-2025 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0023-2025 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.
