By Allison Grande ( September 16, 2010, 6:30 PM EDT) -- Of the nearly 47,000 medical devices cleared by the U.S. Food and Drug Administration's 510(k) review process since 1998, only 77, or 0.16 percent, were involved in a Class I recall between January 2005 and May 2010, a new study by a medical device industry group shows....
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