PlainRecalls
FDA Devices Moderate Class II Ongoing

TourniKwik Tourniquet Set (CFN 79012)

Reported: July 31, 2024 Initiated: May 16, 2024 #Z-2423-2024

Product Description

TourniKwik Tourniquet Set (CFN 79012)

Reason for Recall

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

Details

Units Affected
636 units
Distribution
Worldwide - US Nationwide distribution in the states of MN, MA, UT, CA, and FL. The countries of Japan and Slovenia.
Location
Brooklyn Park, MN

Frequently Asked Questions

What product was recalled?
TourniKwik Tourniquet Set (CFN 79012). Recalled by Medtronic Perfusion Systems. Units affected: 636 units.
Why was this product recalled?
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 31, 2024. Severity: Moderate. Recall number: Z-2423-2024.