Class II — Amtryke LLC
| Recalling firm | AmTryke LLC |
|---|---|
| Registered facility | AMTRYKE LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Product is being recalled due to complaints of cracked frames. |
| Product | AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle. |
| Quantity | 53 units |
| Distribution | US nationwide distribution to AL, CA, FL, HI, IL, KY, KS, LA, MI, NY, OK, OR, PA, SC, TX, VA, VT and WV. |
| Initiated | 2015-03-27 |
| Classified | 2015-04-24 |
| Terminated | 2017-07-10 |
| Recall number | Z-1520-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Amtryke LLC (Z-1520-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/70888/
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