Device recall
Z-0076-2021: CERTAIN BELLATEK TIN ABUTMENT 5.0MM Reference Number: IEDAN5
FDA device recall · Class II · Biomet 3i, LLC
Key facts
| Recall number (Z-number) | Z-0076-2021 |
|---|---|
| Recall event | 86402 |
| Product | CERTAIN BELLATEK TIN ABUTMENT 5.0MM Reference Number: IEDAN5 |
| Product code | NHA |
| Recalling firm | Biomet 3i, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 6, 2022 |
| 510(k) numbers | K052648 |
| 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