FDAJune 1, 2017device

VASER Amplifier, VASER 2.2 VASERlipo System, Rx Only, 115/230V - 60/50Hz 300VA The Vaser amplifier is intended for the fragmentation and emulsification of subcutaneous fatty tissues for aesthetic body contouring (modification of the anatomy).

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

The hazard

Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and 05/23/2017.

What to do

FDA enforcement status: Terminated

Brands named

solta medicalsolta

Recall history

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

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