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INTERSTIM II Adverse Event — Injury (MDR 3004209178-2020-07749)

INTERSTIM II Adverse Event — Injury (MDR 3004209178-2020-07749) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTERSTIM II; Generic name: STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..

DeviceINTERSTIM II
Generic nameSTIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE
ManufacturerMEDTRONIC PUERTO RICO OPERATIONS CO.
Report number3004209178-2020-07749
Event typeInjury
Product problemY
Date received2020-04-27
Report sourceCOMPANY REPRESENTATIVE, HEALTH
NarrativeDATE IS APPROXIMATE. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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