Device recall
Z-0646-2022: Destino Twist 14F (also branded as Guidestar 14F)
FDA device recall · Class II · Oscor Inc.
Key facts
| Recall number (Z-number) | Z-0646-2022 |
|---|---|
| Recall event | 89392 |
| Product | Destino Twist 14F (also branded as Guidestar 14F) |
| Product code | DYB |
| Recalling firm | Oscor Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K140406 |
| FEI number | 1035166 |
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