TourniKwik Tourniquet Set — Class II medical device recall Z-2423-2024
Ongoing recall by Medtronic Perfusion Systems, reported 2024-07-31, distributed nationwide. Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
| Recall number | Z-2423-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Perfusion Systems, Brooklyn Park, MN, United States |
| Recall initiated | 2024-05-16 |
| Classified | 2024-07-23 |
| Reported by FDA | 2024-07-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP, SI |
| Quantity | 636 units |
| UPC / GTIN / UDI-DI | 00673978186269, 20613994576358 |
| Serial numbers | 2023020354, 2023020355, 202304C012, 202305C244 |
| Model numbers | 79012 |
Product
TourniKwik Tourniquet Set (CFN 79012)
Reason for recall
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2423-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.