Device recall
Z-2098-2023: KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used…
FDA device recall · Class II · Pro-Dex Inc
Key facts
| Recall number (Z-number) | Z-2098-2023 |
|---|---|
| Recall event | 92493 |
| Product | KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver |
| Product code | GEY |
| 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