Official recall record
VNS Therapy SenTiva® Duo Generator
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-02-05
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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