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PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR Adverse Event — Malfunction (MDR 1627487-2020-04248)

PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR Adverse Event — Malfunction (MDR 1627487-2020-04248) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR; Generic name: SCS IPG; Manufacturer: ST. JUDE MEDICAL - NEUROMODULATION.

DevicePROCLAIM¿ 5 ELITE IMPLANTABLE PULSE GENERATOR
Generic nameSCS IPG
ManufacturerST. JUDE MEDICAL - NEUROMODULATION
Report number1627487-2020-04248
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, CONSUM
NarrativeDATE OF EVENT IS ESTIMATED. THE RESULTS/ METHOD AND CONCLUSION CODES ALONG WITH INVESTIGATION RESULTS WILL BE PROVIDED IN THE FINAL REPORT.
SourceopenFDA MAUDE (device adverse events)

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