Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to Ortho Kinematics, Inc. notified customers of erroneous results...
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), VMA DataLink Software.2.3.231, 2.3.232. Product Usage: 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. notified customers of erroneous results of VMA tests 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