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EMBLEM MRI S-ICD Adverse Event — Malfunction (MDR 2124215-2020-09152)

EMBLEM MRI S-ICD Adverse Event — Malfunction (MDR 2124215-2020-09152) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EMBLEM MRI S-ICD; Generic name: IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT); Manufacturer: BOSTON SCIENTIFIC CORPORATION.

DeviceEMBLEM MRI S-ICD
Generic nameIMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)
ManufacturerBOSTON SCIENTIFIC CORPORATION
Report number2124215-2020-09152
Event typeMalfunction
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, FOREIG
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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