Ortho Kinematics, Inc: Medical Device Recall in 2018 - (Recall #: Z-2889-2018)

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), 2.3.250. Product System, image processing, radiological

Product Classification:

Class II

Date Initiated: May 23, 2018

Date Posted: August 29, 2018

Recall Number: Z-2889-2018

Event ID: 80769

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.

Status: Ongoing

Product Quantity: 1

Code Information:

00868579000209

Distribution Pattern:

U.S. Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated