FDAAugust 7, 2017device

Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is intended to assist the surgeon in providing software define spatial boundaries for orientation and reference information to anatomical structures during orthopedic procedures.

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

The hazard

Software discrepancy of not showing all the EE constants, when the screen is filled.

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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