Ortho Kinematics, Inc: Medical Device Recall in 2018 - (Recall #: Z-2882-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 11, 2017

Date Posted: August 29, 2018

Recall Number: Z-2882-2018

Event ID: 80680

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.

Status: Ongoing

Product Quantity: 1

Code Information:

UDI: 00868579000209

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated