Device recall
Z-2588-2011: Kinamed SuperCable Grip and Plate System Driver, 3.5mm Hex, Catalog Number…
FDA device recall · Class II · Kinamed Inc
Key facts
| Recall number (Z-number) | Z-2588-2011 |
|---|---|
| Recall event | 58808 |
| Product | Kinamed SuperCable Grip and Plate System Driver, 3.5mm Hex, Catalog Number: 35-860-2060 The driver is intended to be used in conjunction with compression and locking bone screws for fixation of long bone fractures when Kinamed Trochanteric Grips & Cable-Plates are used. Subsequent Product Codes… |
| Product code | KTT |
| Recalling firm | Kinamed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 25, 2011 |
| 510(k) numbers | K072250 |
| FEI number | 2027148 |
At a glance
- 1–9 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