Device recall
Z-1095-2016: Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin…
FDA device recall · Class II · Pro-Dex Inc
Key facts
| Recall number (Z-number) | Z-1095-2016 |
|---|---|
| Recall event | 73034 |
| Product | Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver). |
| Product code | MOQ |
| Recalling firm | Pro-Dex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 21, 2017 |
| FEI number | 2081135 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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