TourniKwik™ 79012Recalls & reported problems
Medtronic, Inc. · TOURNIQUET 79012 TOURNIKWIK 7.5 40PK 17L · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 16, 2024Open, Classified
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.
Z-2423-2024 · Root cause: Under Investigation by firm · FDA record ↗
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- Purstring 020730Covidien LP · CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY46 reports
- Vitality® 07.02100.001Zimmer Spine, Inc. · CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY9 reports
- Endopath E705RJohnson & Johnson Medical GmbH · CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY4 reports
- TourniKwik™ 79011Medtronic, Inc. · CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- Millennium 1-1883Avalign Technologies, Inc. · CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.