Medtronic Perfusion Systems recalls specific left heart vent catheters due to potential shape loss. Affected models include SUCTION 12115 LV VENT 15FR with serial numbers starting 2023051189. Contact for remedy details.
The catheters may not retain their shape.
Medtronic Perfusion Systems is recalling certain left heart vent catheters that may not retain their shape. This could affect medical use and requires checking if your device matches the listed serial numbers.
The catheters may not retain their shape, which could lead to improper function during medical procedures. This might cause issues with blood flow or device effectiveness if the catheter deforms.
Patients using the recalled left heart vent catheters are most at risk. Healthcare providers who have these specific models should verify their devices.
Check for the model number 12115 on the catheter or its packaging. Serial numbers listed in the recall start with 2023051189 and continue through 202403C102. The UDI-DI codes are also listed in the recall.
Look for the serial number on the catheter or its packaging to see if it matches the list provided in the recall.
Reach out to Medtronic Perfusion Systems for further instructions on the recall process.
The model number is SUCTION 12115 LV VENT 15FR.
Check the serial number on the catheter or packaging against the list of numbers provided in the recall (starting with 2023051189).
Contact Medtronic Perfusion Systems for instructions on the recall process.
We’ve drafted a message you can send Medtronic Perfusion Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2482-2025 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-2482-2025 from Medtronic Perfusion Systems. 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.
