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Recall Observatory FDA recall evidence

Device product

VASER PRO Amplifier, VASER 2.2 VASERlipo System stem, 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).

Z-3048-2017

June 01, 2017

Class II

Product summary

Firm
Solta Medical Inc
Event
Event 77655
Status
Terminated
Classification
Class II
Quantity
7 units
Official record key
device-enforcement:Z-3048-2017

Official wording

Reason: 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.

Code information: Reference No. 110-0032; Shipping P/N P007014-03; Device P/N P007023-03; Serial No. 001CW9, 000V1W, 000VBK, VAS10-0135-SB, 001FM0, 000TJ5, 00190Q.

Distribution pattern: US Distribution to the states of : AL, CA, CO, FL, NY, PA, & TX.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.