Fresenius Kabi recalls LVP-0004 infusion pumps due to potential cassette loading lever breakage. Affected units may require replacement to prevent injury.
Potential for the Cassette Loading Lever to break.
Fresenius Kabi is recalling LVP-0004 infusion pumps because the cassette loading lever might break. This could lead to infusion system failure or injury during use.
The cassette loading lever may break during normal use, potentially causing the infusion system to malfunction. This could lead to improper medication delivery or injury if the pump fails unexpectedly.
Patients using the LVP-0004 infusion pumps for medical treatments are affected. Healthcare providers and patients at risk of infusion complications are most vulnerable.
Check for model number LVP-0004 on the pump. The recall applies to pumps sold with UDI-DI: 00811505030320.
Look for model number LVP-0004 on the pump or its packaging.
Reach out to Fresenius Kabi USA, LLC for further assistance or replacement options.
The recall states there is a potential for the cassette loading lever to break, which could cause infusion system failure or injury.
Check for model number LVP-0004 and UDI-DI: 00811505030320 on the pump or its packaging.
Contact Fresenius Kabi USA, LLC for replacement options or further assistance.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-2274-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-2274-2026 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.
