Device recall
Z-1005-03: Profile 8 x 20 mm Cannulated Interference Screw Round Head Catalog Number…
FDA device recall · Class III · Mitek Worldwide
Key facts
| Recall number (Z-number) | Z-1005-03 |
|---|---|
| Recall event | 26503 |
| Product | Profile 8 x 20 mm Cannulated Interference Screw Round Head Catalog Number: 230420 |
| Recalling firm | Mitek Worldwide |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 22, 2003 |
| 510(k) numbers | K982662 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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