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.
- FDAVolcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700, 86700J used with Instructions for use.2025-06-13
- FDAPhilips OmniWire Pressure guide wire REF 89185J PN 3000002528912022-05-16
- FDAVolcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 27972022-05-13
- FDAVolcano Visions PV. 035 Digital IVUS Catheter REF 81234, PN: 300007367341 , Rx Only, Sterile EO, CE 27972022-05-13
- FDAMM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller), Part Numbers: 300002018101, 300002018102, used with IntraSight Integrated (Part Number: 797403) IVUS systems2022-02-03
- FDAIntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 3000020181022022-01-24
- FDASyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x2022-01-19
- FDAPhilips Volcano FFR software used in the following systems connected to the McKesson, Schwarzer, and some Philips Xper Hemodynamic Systems (HMS): (1) Volcano Imaging System s5i, Part #807400001; (2) s5ix Imaging System with s5iz PC Workstation Refurbished, Part#807400001 R and 807401200; (3) s5i ...2018-11-07
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