Related manufacturer report: 1627487-2020-21554, related manufacturer report: 1627487-2020-21555, related manufacturer report: 1627487-2020-21556, related manufacturer report: 1627487-2020-21557, related manufacturer report: 1627487-2020-21558, related manufacturer report: 1627487-2020-21560.It was reported that patient experienced ineffective stimulation.Patient denies any traumas or falls.Programming changes have been attempted prior however was unsuccessful.Device system was explanted.No additional information is available.
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