Device recall
Z-0137-2008: Freedom Designs TriPod w/Anti tipper Manual Wheelchair, Models Numbers: TriPod…
FDA device recall · Class II · Freedom Designs Inc
Key facts
| Recall number (Z-number) | Z-0137-2008 |
|---|---|
| Recall event | 44928 |
| Product | Freedom Designs TriPod w/Anti tipper Manual Wheelchair, Models Numbers: TriPod, Tripod LT and TriPod Pediatric LT with Trailing Anti-Tipper-Caster-Axle Link, Freedom Designs Incorporated, Simi Valley, CA 93065 |
| Product code | IOR |
| Recalling firm | Freedom Designs Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 14, 2008 |
| 510(k) numbers | K060926 |
| FEI number | 2081283 |
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