FDAJanuary 11, 2017device
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.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
ortho kinematicsortho
UPCs
00868579000209
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDAVITROS Chemistry Products CHE Slides (Japan); Catalog Numbers: (1) 684 4074 (90 slides), (2) 684 4138 (300 slides);2025-06-10
- FDABrand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier II Model/Catalog Number: 8231474 Software Version: N/A Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on VITROS 250/350/5,1 FS/...2025-06-10
- FDAVITROS Chemistry Products CHE Slides; Catalog Numbers: (1) 191 4605 (300 slides), (2) 800 4707 (90 slides);2025-06-10
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