Device recall
Z-0960-2017: Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O The…
FDA device recall · Class II · Trilliant Surgical Ltd.
Key facts
| Recall number (Z-number) | Z-0960-2017 |
|---|---|
| Recall event | 76029 |
| Product | Tiger Screw Sterilization Tray Base Assembly Model 210-00-001 Revision N, O The product is a component of a system indicated for the fixation of fractures, non-unions, arthrodeses, and osteotomies of bones appropriate for the size of the device. |
| Product code | HWC |
| Recalling firm | Trilliant Surgical Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2017 |
| 510(k) numbers | K153338 |
| FEI number | 3007420745 |
At a glance
- 1–9 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