Device recall
Z-1391-2023: KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter…
FDA device recall · Class II · Pro-Dex Inc
Key facts
| Recall number (Z-number) | Z-1391-2023 |
|---|---|
| Recall event | 91850 |
| Product | KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter. |
| Product code | GET |
| Recalling firm | Pro-Dex Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2081135 |
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