FDAMarch 22, 2018device

Philips Volcano CORE M2 Vascular System, Part # 400-0100.17, Rx Only. Used for the qualitative and quantitative evaluation of vascular morphology in the coronary arteries and vessels of the peripheral vasculature.

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

The hazard

The incorrect resistor has been used in affected CORE M2 Imaging Systems, which causes noise and results in an overly bright IVUS Image.

What to do

FDA enforcement status: Terminated

Brands named

volcano

UPCs

126620101597126620101599126620101600126620100718126620102313126620102315126620102307126620093077

Recall history

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

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