Z-2183-2012 Class II Terminated
FDA device recall Z-2183-2012 was initiated by JK Products & Services, Inc on May 7, 2012 and is designated Class II. Reason for recall: The Beauty Angel was marketed without a 510k. The recall status is terminated (terminated January 7, 2015). Affected quantity: 598 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 22, 2012
- Initiation Date
- May 7, 2012
- Termination Date
- January 7, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 598 units
Product Description
BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use.
Reason for Recall
The Beauty Angel was marketed without a 510k.
Distribution Pattern
Worldwide Distribution - USA (nationwide) and Canada
Code Information
All Beauty Angel Models and Serial Numbers Part Numbers 80000904301 and 8001110201.