Device recall
Z-0531-2022: 8mm FlexDex Needle Driver, Product Code FD-335 ND
FDA device recall · Class II · FlexDex Inc.
Key facts
| Recall number (Z-number) | Z-0531-2022 |
|---|---|
| Recall event | 89316 |
| Product | 8mm FlexDex Needle Driver, Product Code FD-335 ND |
| Product code | MDM |
| Recalling firm | FlexDex Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2023 |
| FEI number | 3012046682 |
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