Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled by Ortho Kinematics, Inc Due to Ortho Kinematics Inc. sent a Notice of Correction...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ortho Kinematics, Inc directly.
Affected Products
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.
Quantity: 1
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ortho Kinematics, Inc
Ortho Kinematics, Inc has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report