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ACCOLADE MRI DR Adverse Event — Malfunction (MDR 2124215-2020-09226)

ACCOLADE MRI DR Adverse Event — Malfunction (MDR 2124215-2020-09226) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACCOLADE MRI DR; Generic name: IMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT); Manufacturer: BOSTON SCIENTIFIC CORPORATION.

DeviceACCOLADE MRI DR
Generic nameIMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT)
ManufacturerBOSTON SCIENTIFIC CORPORATION
Report number2124215-2020-09226
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceHEALTH PROFESSIONAL
NarrativeAS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED.
SourceopenFDA MAUDE (device adverse events)

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