Ortho Kinematics recalls
Ortho Kinematics has 4 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 29 Aug 2018. 4 are still ongoing. The most frequent reason is device malfunction.
Total recalls4since 2018
Last 12 months0reported
Class I00% of total
Ongoing4latest 29 Aug 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why ortho kinematics is recalled
Product types
By year
Ongoing ortho kinematics recalls
4 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Vertebral Motion Analyzer (VMA) recalled by Ortho Kinematics | Ortho Kinematics | Device Malfunction | Nationwide |
| Device | CLASS II | Vertebral Motion Analyzer (VMA), VMA DataLink recalled | Ortho Kinematics | Device Malfunction | Nationwide |
| Device | CLASS II | Vertebral Motion Analyzer (VMA) recalled by Ortho Kinematics | Ortho Kinematics | Device Malfunction | Nationwide |
| Device | CLASS II | Vertebral Motion Analyzer (VMA) recalled by Ortho Kinematics | Ortho Kinematics | Device Malfunction | Nationwide |
All ortho kinematics recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Vertebral Motion Analyzer (VMA) recalled by Ortho Kinematics | Ortho Kinematics | Device Malfunction | Nationwide |
| Device | CLASS II | Vertebral Motion Analyzer (VMA), VMA DataLink recalled | Ortho Kinematics | Device Malfunction | Nationwide |
| Device | CLASS II | Vertebral Motion Analyzer (VMA) recalled by Ortho Kinematics | Ortho Kinematics | Device Malfunction | Nationwide |
| Device | CLASS II | Vertebral Motion Analyzer (VMA) recalled by Ortho Kinematics | Ortho Kinematics | Device Malfunction | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.