Monthly Archives: December 2011

FDA Classifies Voluntary Physician Advisory Letter on Riata and Riata ST Silicone Defibrillation Leads as Class I Recall

St. Jude Medical, Inc., a global medical device company, recently announced that the U.S. Food and Drug Administration (FDA) has sent its voluntary medical device advisory letter to physicians instituting a Class I Recall regarding the performance of Riata and Riata ST Silicone Defibrillation … Continue reading

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