Device recall
Z-2695-2014: Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr
FDA device recall · Class II · Pdg Product Design Group Inc
Key facts
| Recall number (Z-number) | Z-2695-2014 |
|---|---|
| Recall event | 69035 |
| Product | Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr |
| Product code | IOR |
| Recalling firm | Pdg Product Design Group Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2015 |
| 510(k) numbers | K063736 |
| FEI number | 3002088367 |
At a glance
- 1–9 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