Medtronic recalls TourniKwik Tourniquet Set (CFN 79012) due to incorrect component in some lots. Affected units have specific serial numbers. Consumers should contact Medtronic for details.
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
Medtronic is recalling certain TourniKwik Tourniquet Sets because they contain an incorrect component. This could lead to improper use during medical procedures. Affected units have specific serial numbers and model details.
The recall states that an incorrect component was placed in four manufactured lots of the Tourniquet Set. This could cause improper function during medical procedures, potentially leading to complications if used incorrectly.
Medical professionals and patients using the TourniKwik Tourniquet Set may be affected. Those with the specific serial numbers listed in the recall are most at risk.
Check for the model number 79012 and serial numbers listed: 2023020354, 2023020355, 202304C012, or 202305C244. The UDI codes are also provided for identification.
Verify the model number (79012) and serial numbers listed in the recall to confirm if your product is affected.
The recall states that an incorrect component was placed in four manufactured lots of the TourniKwik Tourniquet Set.
Check for the model number 79012 and serial numbers: 2023020354, 2023020355, 202304C012, or 202305C244.
The recall 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-2423-2024 — Medtronic Perfusion Systems Medtronic Perfusion Systems Hello, I own a Medtronic Perfusion Systems that is covered by recall Z-2423-2024 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.
