VMA 2Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

4 FDA recall records name this device's identifier, 4 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. May 23, 2018Open, Classified

   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.

   Z-2889-2018 · Root cause: Software design · FDA record ↗

2. Mar 2, 2017Open, Classified

   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.

   Z-2891-2018 · Root cause: Software design · FDA record ↗

3. Jan 11, 2017Open, Classified

   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.

   Z-2882-2018 · Root cause: Software Manufacturing/Software Deployment · FDA record ↗

4. Aug 12, 2016Open, Classified

   Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests due to a software bug that has been corrected.

   Z-2890-2018 · Root cause: Software design · FDA record ↗