Fresenius Kabi recalls specific IVENIX infusion sets due to potential serious patient injury from incorrect assembly. Affected units include Lot FA25B03126. Contact for remedy details.
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.
Fresenius Kabi is recalling a specific IVENIX infusion system set that could cause serious patient injury if assembled incorrectly. This recall affects patients receiving IV treatments with the specific lot number.
Incorrect assembly of the specific lot (FA25B03126) can lead to serious patient injury. The hazard occurs during the setup process when the infusion set is not properly connected.
Patients using the recalled IVENIX infusion system set for intravenous treatments are affected. Healthcare providers administering the set are at highest risk.
Check for the product code SET-0032-25 and lot number FA25B03126 on the packaging. The recall applies to the IVENIX Infusion System, LVP Primary Administration Set with dual-inlet and needle-free port features.
Immediately stop using the recalled IVENIX infusion system set if it has the lot number FA25B03126.
The recalled product is the IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25).
Check for the product code SET-0032-25 and lot number FA25B03126 on the packaging.
Immediately stop using it 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 Z-0586-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-0586-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.