FDA Issues a Class I Recall of Vibrational Integrated Bio-photonic Energizer

No Evidence to Support Claims that it Cures Serious, Chronic Illnesses

The FDA has issued 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. This product was manufactured and distributed from November 16, 2002 through March 19, 2008.

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Published on Oct-31-08