Drug recall
Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The…
FDA recall event 87009 · Class II · Mar-Med Co
Key facts
| Event ID | 87009 |
|---|---|
| Recall numbers | Z-0945-2021 |
| Recalling firm | Mar-Med Co |
| Product type | Devices |
| Products | Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The device is intended to be used in surgery on fingers or toes to provide a blood-less field. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A failure can occur if the user attempts to remove the device by partially snipping the edge and pulling on it. The device may tear into two pieces with a portion remaining in place, which can… |
| Initiation date | Dec 28, 2020 |
| Report date | Feb 10, 2021 |
| Termination date | Sep 14, 2023 |
| City | Grand Rapids |
| State | MI |
| Country | United States |
| FEI number | 1832653 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: