Vestibular First Insight Infrared Video Goggles ProRecalls & reported problems
Vestibular First, LLC · The Insight Infrared Video Goggles Pro are intended for viewing and recording eye movements in support of identifying vestibular disorders in patients. The device is intended for use only by a trained healthcare professional in an appropriate healthcare setting. This device provides no diagnoses nor does it provide diagnostic recommendations. The target population is 12+ years of age. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00860002280738), received between Jan 18, 2024 and Jan 18, 2024 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 18, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT CONTACTED VESTIBULAR FIRST ON 22-DEC-2023 AND REPORTED POSSIBLE ALLERGIC REACTION AROUND EYE AREA AFTER ASSESSMENT WITH INSIGHT PRO GOGGLES ON 20-DEC-2023. THE ALLERGIC REACTION WAS NOT AT THE AREAS WHERE THE GOGGLES CONTACT SKIN AT THE FOREHEAD, SIDE OF CHEEKS AND NOSE BRIDGE, BUT WAS AT THE EYE AREA THAT DOES NOT HAVE CONTACT WITH THE GOGGLES (EYELID AND BELOW THE EYE). FACILITY ROUTINELY USES MEMBER'S MARK DISINFECTING WIPES BETWEEN PATIENTS' USE. MSDS FOR MEMBER'S MARK INCLUDES ACTIVE INGREDIENTS ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE AND ALKYL DIMETHYL ETHYL BENZYL AMMONIUM CHLORIDE THAT ARE REPORTED AS IRRITANTS TO THE EYES. VESTIBULAR FIRST RECOMMENDS ONLY 70% ISOPROPYL ALCOHOL FOR DISINFECTING BETWEEN PATIENTS' USE.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 18535371 ↗
Other Nystagmograph devices
- EYE-SYNC X02Neurosync Inc. · Nystagmograph1 recall0 reports
- N/A 27302Medtronic Ps Medical, Inc. · NYSTAGMOGRAPH21 reports
- N/A 27304Medtronic Ps Medical, Inc. · NYSTAGMOGRAPH8 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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