Device recall
Z-1099-2007: Power Linear Cutter Reusable Digital Loading Units with Reloads. Common name…
FDA device recall · Class II · Power Medical Interventions, Inc
Key facts
| Recall number (Z-number) | Z-1099-2007 |
|---|---|
| Recall event | 37982 |
| Product | Power Linear Cutter Reusable Digital Loading Units with Reloads. Common name - Implantable staple. Model number PLC60 |
| Product code | GDW |
| Recalling firm | Power Medical Interventions, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 29, 2007 |
| 510(k) numbers | K052415 |
| FEI number | 3003171713 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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