Ortho Kinematics, Inc: Medical Device Recall in 2018 - (Recall #: Z-2890-2018)

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), VMA DataLink Software.2.3.231, 2.3.232. 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: August 12, 2016

Date Posted: August 29, 2018

Recall Number: Z-2890-2018

Event ID: 80768

Reason for Recall:

Ortho Kinematics, Inc. notified customers of erroneous results of VMA tests due to a software bug that has been corrected.

Status: Ongoing

Product Quantity: 1

Code Information:

00868579000209

Distribution Pattern:

U.S. Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated