Guest guest Posted December 28, 2009 Report Share Posted December 28, 2009 The US Food and Drug Administration (FDA) says, California-based http://visitbulgaria.info/12200-california-company-refuses-recall-its-ozone-gene\ rators Applied Ozone Systems (AOS) has refused to recall its ozone generator devices for treating cancer, AIDS, hepatitis, herpes, other infections and diseases, which the federal health authorities term as unapproved medical devices, which could result in health problems and even death. However, the company's owner states the ozone generators are being sold as water purifiers and not as medical devices, adding his company can only recall something that is broken, not something based on FDA claims. His company, so far has failed to respond to FDA's letter dated 21st December 2009 asking AOS to recall both its AOS-1M ozone generator and AOS-1MD ozone generator devices, selling for $750 and $1,200 on its website, and according to one of its web pages: 'High colonic irrigation kills harmful bacteria, parasites, mould yeast infections and viruses. Draws toxins through blood, liver, lymph back into large intestine for better elimination. It treats the cause, not the symptoms!' Only at the bottom of the web page does the company say the generators are not marketed as medical devices. Under federal law, FDA approval or clearance is required before any device can claim to treat or mitigate diseases, and AOS products FDA says have not been evaluated for their safety and effectiveness for medical purposes. FDA officials state, the insertion of ozone gas into the rectum could cause perforation, bleeding and infection, and inhalation could worsen asthma or pulmonary conditions. Quote Link to comment Share on other sites More sharing options...
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