Device recall
Z-0639-2024: Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and…
FDA device recall · Class II · Zimmer Biomet Spine Inc.
Key facts
| Recall number (Z-number) | Z-0639-2024 |
|---|---|
| Recall event | 93650 |
| Product | Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System |
| Product code | NKB |
| Recalling firm | Zimmer Biomet Spine Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K150896 |
| FEI number | 3012447612 |
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