Drug recall
Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application…
FDA recall event 80680 · Class II · Ortho Kinematics, Inc
Key facts
| Event ID | 80680 |
|---|---|
| Recall numbers | Z-2882-2018 |
| Recalling firm | Ortho Kinematics, Inc |
| Product type | Devices |
| Products | 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. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Jan 11, 2017 |
| Report date | Aug 29, 2018 |
| City | West Lake Hills |
| State | TX |
| Country | United States |
| FEI number | 3006172536 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: