FDA notified healthcare professionals of a Class I Recall of theVibrational Integrated Bio-photonic Energizer (VIBE) Machine Multi-Frequency Electromagnetic Field Generator. This product was manufactured and distributed from November 16, 2002 through March 19, 2008. This device was not been approved by FDA, lacks safety and effectiveness data, and is not manufactured under current good manufacturing practices. The manufacturer 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.