Overview of recall records associated with Kico Knee Innovation Company, including dates, categories and classifications where available.
Classification mix: Class II: 4.
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.
This page summarizes recall records in which the official source identifies Kico Knee Innovation Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
