Device recall
Z-2340-2019: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack…
FDA device recall · Class II · Pro-Dex Inc
Key facts
| Recall number (Z-number) | Z-2340-2019 |
|---|---|
| Recall event | 83113 |
| Product | PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDBP-040-2 Product Usage: -The PDBP-001 Battery is a single use (non-rechargeable) sterile lithium ion battery accessory that powers the PDSD Surgical driver. There… |
| Product code | GEY |
| Recalling firm | Pro-Dex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2022 |
| 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