Blue Belt Technologies recalls

3 official recalls and safety alerts involving Blue Belt Technologies since 2023-10, 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 Blue Belt Technologies or the relevant agency.

  1. 2024-06-19
  2. US
    Drugs & medicalClass II

    Blue Belt Technologies, Inc recalls CORI Starter Kit, Real Intelligence CORI, CORI STARTER KIT - UNIVERSAL.Intended to assist the surgeon in providing software-defined…

    CORI Surgical System with Real Intelligence Software exhibits an increased Marker Registration Error (MRE) which may cause tracker arrays to flicker on screen of the CORI Surgical System during use, and may cause…

    FDA · DeviceBlue Belt Technologies, IncNationwide Foreign: Australia, Austria, Belgium, Brazil, Canada, Chile, China,…Official notice →
  3. 2024-01-17
  4. US
    Drugs & medicalClass II

    Blue Belt Technologies, Inc recalls CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S

    Possibility that the user is unable to resolve drill disconnection error messages.

    FDA · DeviceBlue Belt Technologies, IncDomestic: Nationwide Distribution.Official notice →
  5. 2023-10-11
  6. US
    Drugs & medicalClass II

    Blue Belt Technologies, Inc recalls Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

    CORI software was missing a planning stage that appears in cases of significant knee deformation (outside of the range of 3 degrees valgus to 7 degrees varus) when the surgeon chooses to define the femoral rotational…

    FDA · DeviceBlue Belt Technologies, IncUS Nationwide distribution.Official notice →