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CAPSUREFIX NOVUS LEAD MRI SURESCAN Adverse Event — Malfunction (MDR 3008973940-2020-00997)

CAPSUREFIX NOVUS LEAD MRI SURESCAN Adverse Event — Malfunction (MDR 3008973940-2020-00997) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPSUREFIX NOVUS LEAD MRI SURESCAN; Generic name: ELECTRODE, PACEMAKER, PERMANENT; Manufacturer: MEDTRONIC SINGAPORE OPERATIONS.

DeviceCAPSUREFIX NOVUS LEAD MRI SURESCAN
Generic nameELECTRODE, PACEMAKER, PERMANENT
ManufacturerMEDTRONIC SINGAPORE OPERATIONS
Report number3008973940-2020-00997
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceFOREIGN, HEALTH PROFESSIONAL
NarrativeIF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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