Medtronic recalls specific lots of Custom Perfusion Systems due to potential insufficient welds that could cause leaks. Affected units include lot 221102372 and 221672013 with use by dates 2022-09-21 and 2022-11-02.
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic is recalling specific lots of Custom Perfusion Systems because some units may have been manufactured with insufficient or incomplete welds. This could lead to leaks, which might cause serious complications for patients using the device.
The recall is for specific lots of the Custom Perfusion System that may have been manufactured with insufficient or incomplete welds. This could result in leaks, which might cause serious complications for patients using the device.
Patients using Medtronic Custom Perfusion Systems with the specific lot numbers 221102372 and 221672013 are most at risk. These units were sold with use by dates of September 21, 2022, and November 2, 2022.
Check the lot number on the product label. Affected units include lot 221102372 (use by 2022-09-21) and lot 221672013 (use by 2022-11-02).
Look for the lot number on the product label to determine if it is affected (221102372 or 221672013).
Specific lots may have been manufactured with insufficient or incomplete welds, which could lead to leaks.
Lot numbers 221102372 (use by 2022-09-21) and 221672013 (use by 2022-11-02).
The recall does not specify an immediate stop; however, affected units should be checked for the lot numbers listed.
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-1882-2021 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1882-2021 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.
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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.
