Fresenius Kabi recalls Famotidine injection vials due to microbial contamination and endotoxin testing issues. Affected lots have specific NDC numbers and expiration dates.
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Fresenius Kabi is recalling Famotidine injection vials that may have microbial contamination and endotoxin testing issues. This could pose a risk to patients receiving the medication.
The recall is due to microbial contamination and endotoxin testing results being out of limits. This could lead to infections or adverse reactions in patients receiving the medication.
Patients prescribed Famotidine injection by healthcare providers. Those using the recalled vials for medical treatment are at risk.
Check for NDC numbers 63323-739-11 or 63323-739-12 on the vial. The affected lots are 6133156, 6133194 (expiring 08/2026) and 6133388 (expiring 10/2026).
Identify the NDC number on the vial to determine if it is affected.
Microbial contamination and endotoxin testing results out of limits.
Lots 6133156, 6133194 (expiring 08/2026) and 6133388 (expiring 10/2026).
Look for NDC numbers 63323-739-11 or 63323-739-12 on the vial.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall D-0182-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall D-0182-2026 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.
