Class II

Medical Device Recall: TourniKwik Tourniquet Set (CFN 79012)

Medtronic Perfusion Systems · May 16, 2024

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.

States Affected

NATIONWIDE

Quantity Affected

636 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2423-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Medtronic Perfusion Systems Medical Device Recall: TourniKwik Tourniquet Set (CFN 79012) | SafeCheck