Health Canada — Medical Devices · Canada · 2025-02-05 · Type II
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Reported risk: Complaints have been received on the SenTiva Generator reporting a loss of therapy or inability to make therapy changes with the VNS therapy programming system. A reed switch malfunction, resulting in the reed switch sticking in a closed position has been identified as the cause of these device events. Recall start date: January 10, 2025
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