Device recall
Z-2348-2015: 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical…
FDA device recall · Class II · Zimmer Surgical Inc
Key facts
| Recall number (Z-number) | Z-2348-2015 |
|---|---|
| Recall event | 71575 |
| Product | 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder tourniquet cuffs are generally… |
| Product code | KCY |
| Recalling firm | Zimmer Surgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 4, 2016 |
| FEI number | 1526350 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database