FDANovember 12, 2020device

VNS Therapy SENTIVA DUO # 1000-D - Product Usage: indicated for the treatment of chronic or recurrent depression in patients who are experiencing a treatment-resistant or treatment- intolerant depressive episode.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

During internal testing, it was found that upon a device reset, the Generator exhibits the incorrect Model Number when interrogated.

What to do

FDA enforcement status: Terminated

Brands named

livanova

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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VNS Therapy SENTIVA DUO # 1000-D - Product Usage: indicated for the treatment of chronic or recurrent depression in patients who are experiencing a treatment-resistant or treatment- intolerant depressive episode. — Recall Details · AllClear