medical Class II Updated 2018-08-29

Ortho Kinematics, Inc recalls Vertebral Motion Analyzer (VMA), 2.3.250. Product System,

Recalled Product

Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological

Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 00868579000209
View official government recall

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