Ortho Kinematics, Inc: Medical Device Recall in 2018 - (Recall #: Z-2891-2018)

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), 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.

Product Classification:

Class II

Date Initiated: March 2, 2017

Date Posted: August 29, 2018

Recall Number: Z-2891-2018

Event ID: 80771

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.

Status: Ongoing

Product Quantity: 1

Code Information:

00868579000209.

Distribution Pattern:

U.S. Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated