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Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Recalled August 29, 2018 · FDA recall Z-2889-2018 · Ortho Kinematics
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. · FDA Class II
Units
1
Sold at
U.S. Nationwide Distribution
Description
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.
Product
Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Manufacturer(s)
Ortho Kinematics, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →