Medtronic recalls specific lots of Custom Perfusion Systems due to potential insufficient welds. Affected units may have safety risks.
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic is recalling certain Custom Perfusion Systems that might have been manufactured with weak welds. This could lead to safety issues if the device fails during use.
The device may have insufficient or incomplete welds, which could lead to leaks or failures during use. This might cause the system to malfunction, potentially affecting patient safety.
Patients using the Custom Perfusion System with the specific lot numbers mentioned in the recall are affected. Those who have the device and are at risk of complications from improper welding are most concerned.
Check for the lot number 221238939 on the device packaging or label. The product was sold with the GTIN 00763000286378 and expired by March 3, 2022.
Look for the lot number 221238939 on the device packaging or label.
The recalled device is the Medtronic CB4W67R20 Custom Perfusion System with lot number 221238939.
Check for the lot number 221238939 on the device packaging or label. The product was sold with the GTIN 00763000286378 and expired by March 3, 2022.
The recall record does not specify a remedy, so contact Medtronic directly for further instructions.
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-1881-2021 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1881-2021 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.
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.