Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that included the OVAR research test...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Neuro Kinetics, Inc. directly.
Affected Products
Neuro Kinetics, Inc. (NKI) I-Portal¿ NOTC system with the OVAR research test; a rotary chair system used in vestibular and neuro-otologic diagnostic testing. This device provides no diagnoses nor does it provide diagnostic recommendations.The OVAR test has not yet been cleared by the FDA, and until then can only be used as an investigational device.
Quantity: 45
Why Was This Recalled?
The devices that included the OVAR research test were not cleared for marketing and mTBI research package was sold with the incorrect investigational label.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Neuro Kinetics, Inc.
Neuro Kinetics, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report