Device recall
Z-1168-2024: W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model…
FDA device recall · Class II · W&H DENTALWERK BUERMOOS GMBH
Key facts
| Recall number (Z-number) | Z-1168-2024 |
|---|---|
| Recall event | 93917 |
| Product | W&H Surgical handpiece S-12. For Surgical treatment of dental hard tissue Model Number: 30061000 |
| Product code | KMW |
| Recalling firm | W&H DENTALWERK BUERMOOS GMBH |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K080939 |
| FEI number | 3003755849 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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