Device recall
Z-1324-2020: Abutment Screw Retrieval Kit - Product Usage: The kit itself does not have a…
FDA device recall · Class II · Nobel Biocare Usa Llc
Key facts
| Recall number (Z-number) | Z-1324-2020 |
|---|---|
| Recall event | 84450 |
| Product | Abutment Screw Retrieval Kit - Product Usage: The kit itself does not have a specific intended Use, but included devices have specific intended use as shown above. |
| Product code | DZE |
| Recalling firm | Nobel Biocare Usa Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 15, 2024 |
| 510(k) numbers | K955697 |
| FEI number | 1000125598 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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