Device recall
Z-1802-2020: Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number…
FDA device recall · Class II · Stryker Sustainability Solutions
Key facts
| Recall number (Z-number) | Z-1802-2020 |
|---|---|
| Recall event | 85330 |
| Product | Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868, Reprocessed Tourniquet Cuff - Product Usage: Reprocessed tourniquet cuffs are indicated for use in patients who require surgery of the extremities with an expected duration of less than… |
| Product code | KCY |
| Recalling firm | Stryker Sustainability Solutions |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 14, 2021 |
| FEI number | 3009350690 |
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