Medtronic Perfusion Systems: Medical Device Recall in 2024 - (Recall #: Z-2423-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

TourniKwik Tourniquet Set (CFN 79012)

Product Classification:

Class II

Date Initiated: May 16, 2024

Date Posted: July 31, 2024

Recall Number: Z-2423-2024

Event ID: 94856

Reason for Recall:

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

Status: Ongoing

Product Quantity: 636 units

Code Information:

Model Number: 79012; Serial Number: 2023020354/UDI: 20613994576358, Serial Number: 2023020355/UDI: 00673978186269, Serial Number: 202304C012/UDI: 20613994576358, and Serial Number: 202305C244/UDI: 20613994576358

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of MN, MA, UT, CA, and FL. The countries of Japan and Slovenia.

Voluntary or Mandated:

Voluntary: Firm initiated