Home › RENU MEDICAL, INC › Zimmer Tourniquet
Zimmer Tourniquet
RENU MEDICAL, INC · Model RM-60-7080-103-00 · UDI-DI 00816317023720
KCY
Prescription
10
510(k) clearances
1,989
Adverse events (1 deaths)
47
Recalls
108
Facilities
Description
Zimmer Tourniquet 24 in. DPDB 60-7080-103-00
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-09 | Zimmer Surgical Inc | Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insigni |
| 2026-06-09 | Zimmer Surgical Inc | Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insigni |
| 2026-03-12 | Stryker Sustainability Solutions | Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure. |
| 2025-12-24 | Zimmer Surgical Inc | Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternat |
| 2025-12-24 | Zimmer Surgical Inc | Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternat |
| 2025-07-02 | Stryker Corporation | Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Ot |
| 2024-05-31 | Stryker Sustainability Solutions | Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder. |
| 2023-03-01 | Stryker Corporation | Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, |
| 2023-03-01 | Stryker Sustainability Solutions | Increased incidence of disposable tourniquet cuffs "not able to achieve desired pressure" and "not holding pressure" due to 1) Cuff fabric tearing during use, and 2) Pinched or uns |
| 2023-03-01 | Stryker Corporation | Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.