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INGEVITY MRI Adverse Event — Injury (MDR 2124215-2020-09224)

INGEVITY MRI Adverse Event — Injury (MDR 2124215-2020-09224) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INGEVITY MRI; Generic name: DRUG ELUTING PERMANENT RIGHT VENTRICULAR OR ATRIAL PACEMAKER; Manufacturer: BOSTON SCIENTIFIC CORPORATION.

DeviceINGEVITY MRI
Generic nameDRUG ELUTING PERMANENT RIGHT VENTRICULAR OR ATRIAL PACEMAKER
ManufacturerBOSTON SCIENTIFIC CORPORATION
Report number2124215-2020-09224
Event typeInjury
Product problemN
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE
NarrativeTHERE IS NO ALLEGATION AGAINST THE PERFORMANCE OF THIS PRODUCT. THE PRODUCT IS BEING EVALUATION IN OUR POST MARKET QUALITY ASSURANCE LABORATORY. THIS REPORT WILL BE UPDATED WHEN EVALUATION IS COMPLETE.
SourceopenFDA MAUDE (device adverse events)

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