Kico Knee Innovation Company Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing recall — FDA Z-2292-2026
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.
Overview of recall records associated with Kico Knee Innovation Company, including dates, categories and classifications where available.
Classification mix: Class II: 2.
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.
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.