Medtronic recalls specific lots of Perfusion Systems due to potential insufficient welds. Affected units may have safety risks; contact for return instructions.
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.
The device may have insufficient or incomplete welds, which could lead to failure during use. This might cause the device to malfunction or leak, potentially causing harm to the patient.
Patients using the Medtronic Perfusion Systems with the specific lot numbers mentioned in the recall are affected. Those with the device and the lot numbers listed are at risk.
Check the lot number on your device, which is listed as 221148857 for the affected units. The product includes a use-by date of October 12, 2022, and the GTIN 00643169984820.
Look for the lot number 221148857 on your Medtronic Perfusion System.
The affected lot number is 221148857.
The product was manufactured with a use-by date of October 12, 2022.
Check the lot number on your device; if it is 221148857, it is affected.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1893-2021 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1893-2021 from Medtronic. 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.
