RONAN MEDICAL BrainFeedback Pro 2 Device - is intended as an instrument that provides a recall — FDA Z-2737-2024
Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
Overview of recall records associated with RONAN MEDICAL LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
This page summarizes recall records in which the official source identifies RONAN MEDICAL LLC 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.