Overview of recall records associated with Neuro Kinetics, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
The devices that included the OVAR research test were not cleared for marketing and mTBI research package was sold with the incorrect investigational label.
complaints of system malfunction and unintended, sudden movement at start up. No injuries reported.
This page summarizes recall records in which the official source identifies Neuro Kinetics, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
