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FDA (Device enforcement)Recalled 2024-05-16class ii

Medtronic Perfusion Systems: TourniKwik Tourniquet Set (CFN 79012)

Hazard

Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.

Details from the source

Reason for recall: Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set. Distribution: Worldwide - US Nationwide distribution in the states of MN, MA, UT, CA, and FL. The countries of Japan and Slovenia. Quantity: 636 units Lot/code info: Model Number: 79012; Serial Number: 2023020354/UDI: 20613994576358, Serial Number: 2023020355/UDI: 00673978186269, Serial Number: 202304C012/UDI: 20613994576358, and Serial Number: 202305C244/UDI: 20613994576358

UPC codes

20613994576358, 00673978186269

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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