Device recall
Z-0022-05: iBOT 3000 Mobility System, Independence iBOT 3000 Mobility System…
FDA device recall · Class II · Independence Technology LLC
Key facts
| Recall number (Z-number) | Z-0022-05 |
|---|---|
| Recall event | 29703 |
| Product | iBOT 3000 Mobility System, Independence iBOT 3000 Mobility System (Stair-climbing wheelchair), Class III restricted medical device. |
| Product code | IMK |
| Recalling firm | Independence Technology LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2005 |
| PMA numbers | P020033 |
| FEI number | 3003508375 |
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