EYE-SYNC X02Recalls & reported problems
Neurosync Inc. · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Sep 19, 2023Open, Classified
Eye syncing issues causing the device to be inoperable. Unable to be repaired due to discontinuation of support for the Pico 2 platform, which was no longer in production or serviceable as of August 31, 2023.
Z-2114-2025 · Root cause: Device Design · FDA record ↗
Other Nystagmograph devices
- N/A 27302Medtronic Ps Medical, Inc. · NYSTAGMOGRAPH21 reports
- N/A 27304Medtronic Ps Medical, Inc. · NYSTAGMOGRAPH8 reports
- Vestibular First Insight Infrared Video Goggles ProVestibular First, LLC · Nystagmograph1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.