Device recall
Z-0924-2020: Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041…
FDA device recall · Class II · Jjgc Industria E Comercio De Materials Dentarios Sa
Key facts
| Recall number (Z-number) | Z-0924-2020 |
|---|---|
| Recall event | 84709 |
| Product | Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr. |
| Product code | EJL |
| Recalling firm | Jjgc Industria E Comercio De Materials Dentarios Sa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 1, 2021 |
| FEI number | 3008261720 |
At a glance
- None 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