FDAJune 12, 2015device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is potential risk of electrical shock if lead wires inside the device become detached and the ground connection fails.

What to do

FDA enforcement status: Terminated

Brands named

microaire surgical instrumentsmicroairemicroaire surgical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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