FDA Device recall Z-2891-2018
Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254
- 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), 2.3.239 - 2.3.254 by Ortho Kinematics, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2891-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-03-02 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ortho Kinematics |
| Distribution | US |
Product
Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software application intended to be used to process digital image files.
Reason
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.
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-2891-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.