Device recall
Z-0658-03: Flexgard, off-the-shelf knee brace, product number 14761106
FDA device recall · Class II · De Royal Industries
Key facts
| Recall number (Z-number) | Z-0658-03 |
|---|---|
| Recall event | 25659 |
| Product | Flexgard, off-the-shelf knee brace, product number 14761106 |
| Product code | ITQ |
| Recalling firm | De Royal Industries |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2003 |
| FEI number | 2021791 |
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