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medicine and health
http://EuropeMedicine.blogspot.com
How to save your health and to restore it
- Added on: Jan 14th, 2008
- Country: United States
- Language: English
Recent Posts
FDA Approves Agriflu Seasonal Influenza Vaccine
FDA Approves Agriflu Seasonal Influenza Vaccine Fri, 27 Nov 2009 14:51:00 -0600 The U.S. Food and Drug Administration today approved Agriflu for people ages 18 years and older to prevent disease caused by influenza virus subtypes A and B....
What\'s New at CBER Update
You are subscribed to What's New at CBER for U.S. Food & Drug Administration (FDA). This information has recently been updated, and is now available. Agriflu Posted: 11/27/2009 Manage your FDA Subscriptions: ...
FDA\'s Woodcock Discusses Pain Management and Drug Safety in Nov. 26, 2009 Issue of The New England Journal of Medicine
FDA's Woodcock Discusses Pain Management and Drug Safety in Nov. 26, 2009 Issue of The New England Journal of Medicine Tue, 24 Nov 2009 23:00:00 -0600 An article by Janet Woodcock, M.D., director of the FDA’s Center for Drug Evaluat...
MedWatch - Stryker Operating Room System II Surgical Navigation System: Recall due to potential for the navigation PC SPC-1 component to stop working which could result in potential harms associated with this failure
Stryker Operating Room System II Surgical Navigation System - Recall Audience: Hospital risk managers, surgical service managers Stryker and FDA notified healthcare professionals of a recall of 23...
What\'s New at CBER Update
You are subscribed to What's New at CBER for U.S. Food & Drug Administration (FDA). This information has recently been updated, and is now available. Jobs at the Center for Biologics Evaluation and Research (CBER) Consumer S...
Stryker Corporation\'s Instruments Division Issues Worldwide Class 1 Recall of 23 Operating Room System II Surgical Navigation Systems; Catalog numbers 7700-100-000 and 7700-101-201
Stryker Corporation's Instruments Division Issues Worldwide Class 1 Recall of 23 Operating Room System II Surgical Navigation Systems; Catalog numbers 7700-100-000 and 7700-101-201 Wed, 25 Nov 2009 14:10:00 -0600 Portage, Mich., Nov 4, 20...
Why is "Vibe Machine" a/k/a "The Quantum Pulse" NOT included in the FDA recall? The "Vibe Machine" was conveniently renamed the same machine as "The Quantum Pulse" in response to the FDA investigation leading to this recall. The Vibe machine was determined and predicated by the FDA as an adulterated medical device. To deceive the public without required registering, obtaining Pre Market Approval, and a 510(k) is a mockery to the FDA authority of protecting the public. Could simply changing the name to avoid compliance be a model and license for other companies to endanger the lives of the public by doing the same? If other manufactures have to follow rules with the FDA, then so should Vibe Technologies. They having profited in the millions and millions of dollars allowed this company to comply. There are NO excuses for beating the system.
Posted: November 14th, 2008 | Report This Comment