Device recall
Z-2318-2017: Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque…
FDA device recall · Class II · Zimmer Biomet Spine Inc.
Key facts
| Recall number (Z-number) | Z-2318-2017 |
|---|---|
| Recall event | 77251 |
| Product | Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017 |
| Product code | LYQ |
| Recalling firm | Zimmer Biomet Spine Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 25, 2018 |
| FEI number | 3012447612 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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