Device recall
Z-0890-2022: Customized Brius Appliances (custom metal orthodontic devices); BRIUS, RX Only…
FDA device recall · Class II · Brius Technologies Inc.
Key facts
| Recall number (Z-number) | Z-0890-2022 |
|---|---|
| Recall event | 89569 |
| Product | Customized Brius Appliances (custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL |
| Product code | DYJ |
| Recalling firm | Brius Technologies Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2024 |
| FEI number | 3014680924 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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