PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: September 4, 2024 Initiated: December 11, 2023 #Z-2737-2024

Product Description

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.

Reason for Recall

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

Details

Recalling Firm
RONAN MEDICAL LLC
Units Affected
12
Distribution
Worldwide - US Nationwide distribution in the states of CA, FL, TN, MI, IL, CT and the countries of India.
Location
Colorado Springs, CO

Frequently Asked Questions

What product was recalled?
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.. Recalled by RONAN MEDICAL LLC. Units affected: 12.
Why was this product recalled?
Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 4, 2024. Severity: Moderate. Recall number: Z-2737-2024.