FDA Device recall Z-2889-2018
Vertebral Motion Analyzer (VMA), 2.3.250
- FDA Device
- Class II
- ongoing
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of Vertebral Motion Analyzer (VMA), 2.3.250 by Ortho Kinematics, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2889-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-05-23 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ortho Kinematics |
| Distribution | US |
Product
Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Reason
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.
Identifiers
| code_info | 00868579000209 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2889-2018%22
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