FDADecember 27, 2017device

Makoplasty RIO Standard System; Ethernet to Fiber Optic Converter Catalog # 200933 Product Usage: The Partial Knee Application (PKA), for use with the Mako System, is indicated for use in surgical knee procedures, in which the use of stereotactic surgery may be appropriate, and where reference to...

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

The hazard

Communication-connection error.

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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Makoplasty RIO Standard System; Ethernet to Fiber Optic Converter Catalog # 200933 Product Usage: The Partial Knee Application (PKA), for use with the Mako System, is indicated for use in surgical knee procedures, in which the use of stereotactic surgery may be appropriate, and where reference to... — Recall Details · AllClear