Device recall
Z-316/318-3: Drop Hooks for Xact (tm) Lo-Pro with Removeable Drop Seat, Xact Integrated, and…
FDA device recall · Class II · Action Products Incorporated
Key facts
| Recall number (Z-number) | Z-316/318-3 |
|---|---|
| Recall event | 25070 |
| Product | Drop Hooks for Xact (tm) Lo-Pro with Removeable Drop Seat, Xact Integrated, and Xact Individual with Integrated Drop Seat wheelchairs, model/item numbers 05D, 1D, and 15D. Packaged as set of four in a poly bag. |
| Product code | KNO |
| Recalling firm | Action Products Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 10, 2002 |
| FEI number | 1181047 |
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