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EVERA MRI XT DR SURESCAN Adverse Event — Injury (MDR 3004209178-2020-07806)

EVERA MRI XT DR SURESCAN Adverse Event — Injury (MDR 3004209178-2020-07806) 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 number3004209178-2020-07806
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceHEALTH PROFESSIONAL
NarrativeIF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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