PlainRecalls
FDA Devices Moderate Class II Terminated

ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.

Reported: October 7, 2015 Initiated: June 12, 2015 #Z-2822-2015

Product Description

ASP-1021 LipoTower with Aspiration Pump and Tumescent 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.

Details

Units Affected
168, ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump
Distribution
Nationwide Distribution.
Location
Charlottesville, VA

Frequently Asked Questions

What product was recalled?
ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.. Recalled by MicroAire Surgical Instruments, LLC. Units affected: 168, ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump.
Why was this product recalled?
There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 7, 2015. Severity: Moderate. Recall number: Z-2822-2015.