# FDA recall Z-2891-2018

> **Ortho Kinematics, Inc** · Class II · device recall initiated 2017-03-02.

## 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 for recall

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.

## Distribution

U.S. Nationwide Distribution

## Key facts

- **Recall number:** Z-2891-2018
- **Recalling firm:** Ortho Kinematics, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-03-02
- **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-2891-2018

## Citation

> AI Analytics. FDA recall Z-2891-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2891-2018. Source: US FDA. Licensed CC0.

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