Vertebral Motion Analyzer — Class II medical device recall Z-2889-2018
Ongoing recall by Ortho Kinematics, Inc, reported 2018-08-29, distributed nationwide. This email is to provide notification that, due to a software bug that has been corrected, the Radiological Re
| Recall number | Z-2889-2018 |
|---|---|
| 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 | 2018-05-23 |
| Classified | 2018-08-22 |
| Reported by FDA | 2018-08-29 |
| Distributed | Nationwide (US) |
| Quantity | 1 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00868579000209 |
Product
Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Reason for recall
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.
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-2889-2018. 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.