FDASeptember 22, 2021device
ROSA One 3.1 Brain application The device is intended for the spatial positioning and orientation of instruments holders or tool guides to be used by trained surgeons to guide standard surgical instruments during brain and spine surgeries.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain application which led to the inaccurate placement of an electrode during surgery. The firm has received 3 global complaints related to the issue. An incorrect trajectory could result in serious injury or death if undetected during surgery.
What to do
FDA enforcement status: Ongoing
Brands named
medtech sasmedtech
Recall history
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