FDADecember 11, 2023device

BrainFeedback Pro 2 Device - is intended as an instrument that provides a visual and auditory signal corresponding to the status of a patients physiological parameters so that the patient can control voluntarily these physiological parameters.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.

What to do

FDA enforcement status: Ongoing

Brands named

ronan medicalronan

UPCs

0859256600101708592566001123

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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