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CLARIA MRI QUAD CRT-D SURESCAN Adverse Event — Injury (MDR 3004209178-2020-07734)

CLARIA MRI QUAD CRT-D SURESCAN Adverse Event — Injury (MDR 3004209178-2020-07734) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CLARIA MRI QUAD CRT-D SURESCAN; Generic name: DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARD; Manufacturer: MEDTRONIC PUERTO RICO OPERA

DeviceCLARIA MRI QUAD CRT-D SURESCAN
Generic nameDEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARD
ManufacturerMEDTRONIC PUERTO RICO OPERATIONS CO.
Report number3004209178-2020-07734
Event typeInjury
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeCONCOMITANT MEDICAL PRODUCTS: 694765, LEAD, IMPLANTED: (B)(6) 2009. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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