Fresenius Kabi recalls specific ketamine HCl injections due to lack of sterility assurance. Affected lots may cause infections if used. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
Fresenius Kabi is recalling certain ketamine HCl injections that may not be sterile, posing a risk of infection. This recall affects specific lots with expiration dates through April 2026. Users should stop using these products and contact the manufacturer for guidance.
The injections lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If used, this could lead to infections or other health complications.
Healthcare professionals and patients using the recalled ketamine injections for medical purposes. Those with the specific lot numbers listed are most at risk.
Check the product label for the lot numbers: C274-000047883 (exp 17-Feb-26), C274-000048515 (exp 22-Mar-26), C274-000048679 (exp 31-Mar-26), C274-000049119 (exp 19-Apr-26), or C274-000049282 (exp 27-Apr-26).
Immediately stop using the recalled ketamine HCl injections with the specified lot numbers.
Ketamine HCl injections with the lot numbers: C274-000047883 (exp 17-Feb-26), C274-000048515 (exp 22-Mar-26), C274-000048679 (exp 31-Mar-26), C274-000049119 (exp 19-Apr-26), or C274-000049282 (exp 27-Apr-26).
Check the product label for the lot numbers listed above. If your product matches one of these lot numbers, it is affected.
Immediately stop using the product and 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-0334-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0334-2026 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.
