Vertebral Motion Analyzer — Class II medical device recall Z-2882-2018
Ongoing recall by Ortho Kinematics, Inc, reported 2018-08-29, distributed nationwide. Ortho Kinematics Inc. sent a Notice of Correction to Released Testing Results, Radiological Read Report for th
| Recall number | Z-2882-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ortho Kinematics, Inc, West Lake Hills, TX, United States |
| Recall initiated | 2017-01-11 |
| Classified | 2018-08-21 |
| Reported by FDA | 2018-08-29 |
| Distributed | Nationwide (US) |
| Quantity | 1 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00868579000209 |
Product
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2882-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.