Fresenius Kabi recalls LVP Primary Administration Sets with Product Code SET-0013-25 due to potential medication overdose risk. Affected units may cause dose errors during IV infusion.
A defect may cause an uncontrolled medication flow condition which may result in a dose greater than prescribed for the patient (i.e., medication overdose).
Fresenius Kabi is recalling LVP Primary Administration Sets that could cause medication overdoses if used incorrectly. This is serious because it might lead to harmful doses of IV medication.
The device may allow medication to flow uncontrollably, leading to higher doses than prescribed. This could cause overdose if the flow rate is not properly managed during IV infusion.
Patients using the recalled LVP Primary Administration Sets for intravenous infusion are at risk. Healthcare providers administering IV medications with these sets should stop use immediately.
Check for Product Code SET-0013-25 on the packaging. The lot number 3010538 is associated with this specific recall batch.
Immediately stop using the recalled LVP Primary Administration Sets with Product Code SET-0013-25 to prevent medication overdose.
The product code is SET-0013-25.
Check for Product Code SET-0013-25 on the packaging or Lot number 3010538.
The recall record does not mention any remedy or fix.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-2721-2024 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-2721-2024 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.