Reported Aug 29, 2018 · Ongoing
Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Ortho Kinematics, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Ortho Kinematics, Inc · 110 Wild Basin Rd Ste 250 · West Lake Hills, TX · 78746-3352
Is this the product you have?
- Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
- Lot codes and dates
- 00868579000209
- Amount recalled
- 1
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Ortho Kinematics, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.