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Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software a
Recalled August 29, 2018 · FDA recall Z-2891-2018 · Ortho Kinematics
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. · FDA Class II
Units
1
Sold at
U.S. Nationwide Distribution
Description
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.
Product
Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software application intended to be used to process digital image files.
Manufacturer(s)
Ortho Kinematics, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →