FDANovember 29, 2018device

Sensis Vibe System, Model Number 11007642, with software version VD10B.

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

The hazard

A software error may result in a system crash. The system must be restarted before the clinical procedure can be continued. The ablation treatment must be performed with a different system or without the use of the interface.

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

Recall history

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

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Sensis Vibe System, Model Number 11007642, with software version VD10B. — Recall Details · AllClear