← DeviceEvents
HomeDevice Adverse Events

EVERA MRI XT DR SURESCAN Adverse Event — Injury (MDR 3004209178-2020-07724)

EVERA MRI XT DR SURESCAN Adverse Event — Injury (MDR 3004209178-2020-07724) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EVERA MRI XT DR SURESCAN; Generic name: DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..

DeviceEVERA MRI XT DR SURESCAN
Generic nameDEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER
ManufacturerMEDTRONIC PUERTO RICO OPERATIONS CO.
Report number3004209178-2020-07724
Event typeInjury
Product problemY
Date received2020-04-27
Report sourceCONSUMER
NarrativeIF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

🔍 Search all device adverse events →