Z-1520-2015 Class II Terminated
FDA device recall Z-1520-2015 was initiated by Amtryke LLC on March 27, 2015 and is designated Class II. Reason for recall: Product is being recalled due to complaints of cracked frames. The recall status is terminated (terminated July 10, 2017). Affected quantity: 53 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 6, 2015
- Initiation Date
- March 27, 2015
- Termination Date
- July 10, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 53 units
Product Description
AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
Reason for Recall
Product is being recalled due to complaints of cracked frames.
Distribution Pattern
US nationwide distribution to AL, CA, FL, HI, IL, KY, KS, LA, MI, NY, OK, OR, PA, SC, TX, VA, VT and WV.
Code Information
Model: 1424, System number 50-HC-1424, Batch number 2-1301 and GM-0314.