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ADVANCECE Adverse Event — Malfunction (MDR 1220452-2020-00043)

ADVANCECE Adverse Event — Malfunction (MDR 1220452-2020-00043) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ADVANCECE; Generic name: CATHETER, EMBOLECTOMY; Manufacturer: MEDTRONIC, INC.

DeviceADVANCECE
Generic nameCATHETER, EMBOLECTOMY
ManufacturerMEDTRONIC, INC
Report number1220452-2020-00043
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, FOREIG
NarrativeIF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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