RegWardenFDA facility compliance records
Company

Kico Knee Innovation Company

3 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2025: 1 recalls; 2026: 2 recalls201720182019202020212022202320241202522026
  • Recalls (3)

Registered facilities (2)

Recalls & enforcement

  • Class IIOngoing2026-07-13
    Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
  • Class IIOngoing2026-04-23
    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.
  • Class IIOngoing2025-09-19
    Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “Kico Knee Innovation Company — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10054916-kico-knee-innovation-company/

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