-----Original
Message-----
From: U.S. Food & Drug Administration (FDA)
[mailto:fda@service.govdelivery.com]
Sent: Friday, October 31, 2008 5:45 PM
To: (blanked)
Subject: FDA MedWatch- Vibe Technologies Vibrational Integrated
Bio-photonic Energizer Machine Multi-Frequency Field Generator- Class I
Recall
Because Of Unsupported Claims
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|
Vibe Technologies
Vibrational Integrated Bio-photonic
Energizer Machine Multi-Frequency Field Generator
Audience: Healthcare professionals
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.
Read the entire 2008 MedWatch
Safety
Summary, including a link to the FDA Recall notice regarding this issue
at:
http://www.fda.gov/medwatch/safety/2008/safety08.htm#Vibe
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