FDA Medical Device Recalls (openFDA)
Amtryke LLC: AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
- Recall number
- Z-1520-2015
- Recalling firm
- Amtryke LLC
- Product
- AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
- Status
- Terminated
- Initiated
- 2015-03-27
- Posted
- 2015-04-24
- Terminated
- 2017-07-10
- Reason
- Product is being recalled due to complaints of cracked frames.
- Root cause
- Under Investigation by firm
- Action
- Consignees were notified via letter on 03/27/2015.
- 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.
- Lot, serial or model codes
- Model: 1424, System number 50-HC-1424, Batch number 2-1301 and GM-0314.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- ION
- Firm FEI
- 3009020186
- Firm city
- Greensboro
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28