Device recall
Z-0928-06: Model Number: GNRADIOLUCENTGUIDE (Gliding Nail Radiolucent Guide), instrument…
FDA device recall · Class II · Plus Orthopedics USA
Key facts
| Recall number (Z-number) | Z-0928-06 |
|---|---|
| Recall event | 35054 |
| Product | Model Number: GNRADIOLUCENTGUIDE (Gliding Nail Radiolucent Guide), instrument set that contains one unit of each of the following instrument: 1130020-A: GNp Carbon Targeting Handle 1130021-A: GN Adapter Screw for Handle SW 10 1130022-A: GN Targeting Guide Carbon 125 1130023-A: GN Targeting Guide… |
| Product code | KTT |
| Recalling firm | Plus Orthopedics USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2007 |
| FEI number | 3001237832 |
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