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Mako Surgical Corporation recalls MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software de
Recalled July 26, 2017 · FDA recall Z-2741-2017 · Mako Surgical
Hazard
An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection. · FDA Class II
Units
20
Sold at
Distributed to the states of AZ, CA, CO, CT, FL, GA, ID, LA, MA, MO, MS, NC, OH, PA, TN, TX, & WA.
Description
An intermittent electrical problem that could lead to a loss of system power due to a loose screw connection.
Product
MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software defined spatial boundaries during orthopedic procedures.
Manufacturer(s)
Mako Surgical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →