Recall Z-1520-2015— Amtryke LLC
Class II · Terminated
Class II FDA medical device recall by Amtryke LLC, initiated 2015-03-27, terminated 2017-07-10. FDA's recall record names no specific 510(k) clearance for this event. Product: AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.. Reason: Product is being recalled due to complaints of cracked frames..
- Recalling firm
- Amtryke LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-03-27
- Terminated
- 2017-07-10
- Firm location
- Greensboro, NC, United States
Product description
AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
Reason for recall
Product is being recalled due to complaints of cracked frames.
Data sourced from openFDA. This site is unofficial and independent of the FDA.