FDAJanuary 22, 2015device

Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System (RIO), is indicated for use in surgical knee procedures.

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

The hazard

When using the MAKOplasty partial knee Arthroplasty application, the burr continues spinning outside of the stereotactic boundary and after the control switches (foot pedal and trigger) cease to be activated

What to do

FDA enforcement status: Terminated

Brands named

mako surgicalmako

Recall history

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

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