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U.S. Department of Health and Human Services

Safety

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Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator

Audience: Healthcare professionals

[Posted 10/31/2008] FDA notified healthcare professionals of a Class I Recall of the Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator. This device has not been approved by FDA, lacks safety and effectiveness data, and is not manufactured under current good manufacturing practices. The manufacturer has submitted no evidence to FDA to support any of their claims that the product could treat or cure such diseases as cancer, depression, infection and pain. Individuals with the device should stop using it immediately and contact the manufacturer to make arrangements to return the device.

[December 15, 2008 - News Release - FDA]
[October 31, 2008 - Recall Notice - FDA]