Recall Atlas

Kico Knee Innovation recalls

4 official recalls and safety alerts involving Kico Knee Innovation since 2025-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Kico Knee Innovation or the relevant agency.

  1. 2026-08-26
  2. US
    Drugs & medicalClass II

    Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Software…

    Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing

    FDA · DeviceKico Knee Innovation CompanyConsignee Consignee Number Region Device Quantity RFK MEDICAL CE102 RICHMOND…Official notice →
  3. 2026-06-10
  4. US
    Drugs & medicalClass II

    Kico Knee Innovation Company recalls Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly;…

    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.

    FDA · DeviceKico Knee Innovation CompanyWorldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI,…Official notice →
  5. US
    Drugs & medicalClass II

    Kico Knee Innovation Company recalls Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly;…

    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.

    FDA · DeviceKico Knee Innovation CompanyWorldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI,…Official notice →
  6. 2025-10-22
  7. US
    Drugs & medicalClass II

    Kico Knee Innovation Company recalls Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version:…

    Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.

    FDA · DeviceKico Knee Innovation CompanyUS Nationwide distribution in the states of IN, MN, MO, OH, FL, IL, RI, KY,…Official notice →