Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion Systems Due to Incorrect component placed in four manufactured lots of...

Date: May 16, 2024
Company: Medtronic Perfusion Systems
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Perfusion Systems directly.

Affected Products

TourniKwik Tourniquet Set (CFN 79012)

Quantity: 636 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Medtronic Perfusion Systems

Medtronic Perfusion Systems has 96 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report