FDA Device recall Z-1520-2015
AmTryke Model 1424 Community Cruiser Hand Cycle
- FDA Device
- Class II
- terminated
- Published 2015-05-06
On 2015-05-06 the FDA classified a Class II recall of AmTryke Model 1424 Community Cruiser Hand Cycle by Amtryke, citing product is being recalled due to complaints of cracked frames.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1520-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-27 |
| Published | 2015-05-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Amtryke |
| Distribution | US |
Product
AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
Reason
Product is being recalled due to complaints of cracked frames.
Identifiers
| code_info | Model: 1424, System number 50-HC-1424, Batch number 2-1301 and GM-0314. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1520-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.