Device recall
Z-3206-2017: ABUT GOLD FRICTION-FIT, REF HLA3G; ABUT GOLD FRICTION-FIT, REF HLA4G; COPING…
FDA device recall · Class II · Zimmer Dental Inc
Key facts
| Recall number (Z-number) | Z-3206-2017 |
|---|---|
| Recall event | 77911 |
| Product | ABUT GOLD FRICTION-FIT, REF HLA3G; ABUT GOLD FRICTION-FIT, REF HLA4G; COPING GOLD ENG 5.7 MM, REF HLA5G; COPING GOLD NON-ENG. 3.5, REF NEA3G; COPING GOLD NON-ENG. 4.5, REF NEA4G |
| Product code | DZE |
| Recalling firm | Zimmer Dental Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 5, 2019 |
| 510(k) numbers | K011028, K013227 |
| FEI number | 1038806 |
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