Device recall
Z-1356-2020: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual…
FDA device recall · Class II · Zimmer Surgical Inc
Key facts
| Recall number (Z-number) | Z-1356-2020 |
|---|---|
| Recall event | 84752 |
| Product | Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical professionals to exert enough… |
| Product code | KCY |
| Recalling firm | Zimmer Surgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 30, 2020 |
| 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