Medtronic recalls specific lots of Perfusion Systems due to potential insufficient welds. Affected units may have safety risks; contact for remedy details.
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic is recalling specific lots of Perfusion Systems that may have been manufactured with insufficient or incomplete welds. This could lead to safety issues if the device fails during use.
Insufficient welds in the device could cause it to fail during use, potentially leading to safety issues. This is a manufacturing defect that may not cause immediate harm but requires attention to prevent potential failure.
Users of the Medtronic Perfusion Systems with the specific lot numbers mentioned in the recall are affected. Patients using these devices for medical purposes are at the highest risk.
Check for the lot number 221227814 on the device packaging or label. The product was sold with a use-by date of August 28, 2022, and the GTIN 00763000467449.
Look for the lot number 221227814 on the device packaging or label.
The affected lot number is 221227814.
The recall record does not specify a remedy, so contact Medtronic for further instructions.
The product was sold with a use-by date of August 28, 2022.
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-1883-2021 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-1883-2021 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.