| Subject: | Class I Recall For Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-Frequency Field Generator |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 3 Nov 2008 - 10:00 am |
| The FDA has notified healthcare professionals of a Class I Recall of the Vibe Technologies Vibrational Integrated Bio-photonic Energizer Machine Multi-frequency Field Generator. The company's labeling reported that the device could be used to treat or cure medical conditions and diseases such as cancer, depression, infection, and pain. This device has not been approved by FDA, lacks safety and effectiveness data, and is not manufactured under current good manufacturing practices. The... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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