FDA Classifies Riata and Riata ST Silicone Defibrillation Leads as Class I Recall
Posted by on January 7, 2012
The FDA has classified this recall as a Class I recall because of the potential risk of serious injury or patient death if affected devices malfunction.
Finish Reading: FDA Classifies Riata and Riata ST Silicone Defibrillation Leads as Class I Recall
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Tags: Class, Classifies, Defibrillation, Leads, Recall, Riata, Silicone
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