FDAJune 7, 2017device

MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.

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

The hazard

An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.

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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MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures. — Recall Details · AllClear