Z-2821-2015 Class II Terminated
FDA device recall Z-2821-2015 was initiated by MicroAire Surgical Instruments, LLC on June 12, 2015 and is designated Class II. Reason for recall: There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails. The recall status is terminated (terminated May 23, 2016). Affected quantity: 3 LipoTower with Aspiration Pump.
Recall Details
- Product Type
- Devices
- Report Date
- October 7, 2015
- Initiation Date
- June 12, 2015
- Termination Date
- May 23, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3 LipoTower with Aspiration Pump
Product Description
ASP-1020 LipoTower with Aspiration Pump. Medical use.
Reason for Recall
There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Distribution Pattern
Nationwide Distribution.
Code Information
Serial numbers 14031102, 15021105, and 14101103.