Fresenius Kabi recalls blood administration sets with potential for external cassette leaks. Affected units include specific product codes and lot numbers. Consumers should contact the company for details.
Potential for external cassette leaks
Fresenius Kabi is recalling blood administration sets that could leak externally. This hazard might cause contamination or infection if blood leaks outside the intended system.
The sets have a potential for external leaks from the cassette. If blood leaks outside the intended system, it could lead to contamination or infection risks.
People using blood administration sets for medical treatments. Those with specific product codes and lot numbers are most at risk.
Check for product code SET-0014-20 and lot numbers FA24K05023, FA24L02010, FA24L04198, or FA24L04214. These units were sold with the specific product name.
Look for product code SET-0014-20 and lot numbers FA24K05023, FA24L02010, FA24L04198, or FA24L04214.
Contact Fresenius Kabi USA, LLC for instructions on how to handle the recalled product.
The recall states potential for external leaks, but no specific serious injury mechanism is described.
Check for product code SET-0014-20 and lot numbers FA24K05023, FA24L02010, FA24L04198, or FA24L04214.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-2233-2025 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-2233-2025 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.
