# FDA recall Z-2882-2018

> **Ortho Kinematics, Inc** · Class II · device recall initiated 2017-01-11.

## 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.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2882-2018
- **Recalling firm:** Ortho Kinematics, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-01-11
- **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-2882-2018

## Citation

> AI Analytics. FDA recall Z-2882-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2882-2018. Source: US FDA. Licensed CC0.

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