# FDA recall Z-2889-2018

> **Ortho Kinematics, Inc** · Class II · device recall initiated 2018-05-23.

## 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.

## Distribution

U.S. Nationwide Distribution

## Key facts

- **Recall number:** Z-2889-2018
- **Recalling firm:** Ortho Kinematics, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-05-23
- **Report date:** 2018-08-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Lake Hills, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2889-2018

## Citation

> AI Analytics. FDA recall Z-2889-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2889-2018. Source: US FDA. Licensed CC0.

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