Medtronic Perfusion Systems recalls DLP Left Heart Vent Catheter Model 12113 due to potential shape loss. Affected units sold in 2023-2024 with specific serial numbers. Contact for replacement or return.
The catheters may not retain their shape.
Medtronic Perfusion Systems is recalling DLP Left Heart Vent Catheters with model number 12113 because they may not retain their shape. This could lead to improper function during medical procedures. Patients using these catheters should contact Medtronic for guidance.
The catheters may not retain their shape, which could cause improper function during medical procedures. This might lead to complications if the device does not stay in the correct position in the heart.
Patients using the DLP Left Heart Vent Catheter Model 12113 with specific serial numbers from 2023 to 2024 are affected. Those with the catheter for heart procedures are at risk if the device loses shape.
Check for the model number 12113 on the catheter. Affected units have serial numbers listed in the recall notice, including those starting with 2023051188 through 202407C109.
Look for the specific serial numbers listed in the recall notice to confirm if your catheter is affected.
The catheters may not retain their shape, which could cause improper function during medical procedures.
The recall notice does not specify a remedy; contact Medtronic directly for guidance.
Yes, affected units have serial numbers starting with 2023051188 through 202407C109 as listed in the recall notice.
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-2480-2025 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-2480-2025 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.
