FDAOctober 11, 2016device

ROSA Brain, 3.0.0 The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device is indicated for any neurosu...

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

The hazard

Complaint of the head holder connector locking up mechanically when tightened.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

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

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