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Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application intende
Recalled August 29, 2018 · FDA recall Z-2882-2018 · Ortho Kinematics
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. · FDA Class II
Units
1
Sold at
US Nationwide Distribution
Description
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.
Product
Vertebral Motion Analyzer (VMA) Version 2.3.252. 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 →