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Vibe Technologies recall

This article was originally published in The Gray Sheet

Executive Summary

Recall initiated Oct. 1 of Vibe Technologies' Vibrational Integrated Bio-photonic Energizer (VIBE) multi-frequency electromagnetic field generator is Class I, FDA says Oct. 31. The firm claims the device can treat or cure cancer, depression, infection and pain. However, it has not been approved by FDA. The company warns customers to stop using the device. The recall follows an April 11 warning letter from FDA for marketing the unapproved system
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