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CAPSUREFIX NOVUS LEAD MRI SURESCAN Adverse Event — Malfunction (MDR 2649622-2020-08428)

CAPSUREFIX NOVUS LEAD MRI SURESCAN Adverse Event — Malfunction (MDR 2649622-2020-08428) 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: MPRI.

DeviceCAPSUREFIX NOVUS LEAD MRI SURESCAN
Generic nameELECTRODE, PACEMAKER, PERMANENT
ManufacturerMPRI
Report number2649622-2020-08428
Event typeMalfunction
Product problemY
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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