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Ortho Kinematics Recalls
4 recalls on record · August 29, 2018 to August 29, 2018 · Medical Devices
August 29, 2018Medical DevicesFDA
Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software a
Hazard: Ortho Kinematics notified customers that errors were contained in Radiological Read Report and VMA Report for the VMA test. The error resulted from an administrative error of VMA user account settings and has been fixed.
August 29, 2018Medical DevicesFDA
Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA), VMA DataLink Software.2.3.231, 2.3.232. Product Usage: VMA software is a quantitat
Hazard: Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests due to a software bug that has been corrected.
August 29, 2018Medical DevicesFDA
Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Hazard: This email is to provide notification that, due to a software bug that has been corrected, the Radiological Read Report for the VMA test(s) contained an error.
August 29, 2018Medical DevicesFDA
Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application intende
Hazard: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing Results, Radiological Read Report for the Vertebral Motion Analyzer (VMA) test because it contained an error. The error occurred due to a software bug that has been corrected.