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PIONEER PLUS CATHETER Adverse Event — Malfunction (MDR 2939520-2020-00013)

PIONEER PLUS CATHETER Adverse Event — Malfunction (MDR 2939520-2020-00013) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PIONEER PLUS CATHETER; Generic name: CATHETER FOR CROSSING TOTAL OCCULUSIONS; Manufacturer: PHILIPS VOLCANO.

DevicePIONEER PLUS CATHETER
Generic nameCATHETER FOR CROSSING TOTAL OCCULUSIONS
ManufacturerPHILIPS VOLCANO
Report number2939520-2020-00013
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeINTERNAL REFERENCE: (B)(4). THIS CASE WAS REVIEWED, AND INVESTIGATED ACCORDING TO THE MANUFACTURERS POLICY. FACILITY DECLINED TO PROVIDE PATIENT INFORMATION. NO INFORMATION AVAILABLE. THE IMPLANT OR EXPLANT DATES ARE NOT APPLICABLE TO THIS DEVICE.
SourceopenFDA MAUDE (device adverse events)

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