Device recall
Z-1520-2015: AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
FDA device recall · Class II · Amtryke LLC
Key facts
| Recall number (Z-number) | Z-1520-2015 |
|---|---|
| Recall event | 70888 |
| Product | AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle. |
| Product code | ION |
| Recalling firm | Amtryke LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 10, 2017 |
| FEI number | 3009020186 |
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