Device recall
Z-0309-05: Titanium Orthos Bracket
FDA device recall · Class II · Ormco Corporation
Key facts
| Recall number (Z-number) | Z-0309-05 |
|---|---|
| Recall event | 30515 |
| Product | Titanium Orthos Bracket |
| Product code | EJF |
| Recalling firm | Ormco Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 17, 2005 |
| FEI number | 2016150 |
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