FDA Device recall Z-2423-2024
TourniKwik Tourniquet Set (CFN 79012)
- FDA Device
- Class II
- ongoing
- Published 2024-07-31
On 2024-07-31 the FDA classified a Class II recall of TourniKwik Tourniquet Set (CFN 79012) by Medtronic Perfusion Systems, citing incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2423-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-16 |
| Published | 2024-07-31 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | US |
Product
TourniKwik Tourniquet Set (CFN 79012)
Reason
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
Identifiers
| code_info | Model Number: 79012; Serial Number: 2023020354/UDI: 20613994576358, Serial Number: 2023020355/UDI: 00673978186269, Seri…Model Number: 79012; Serial Number: 2023020354/UDI: 20613994576358, Serial Number: 2023020355/UDI: 00673978186269, Serial Number: 202304C012/UDI: 20613994576358, and Serial Number: 202305C244/UDI: 20613994576358 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2423-2024%22
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