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U.S. Department of Health and Human Services

Safety

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PHOTO - FDA Classifies Voluntary Physician Advisory Letter on Riata and Riata ST Silicone Defibrillation Leads as Class I Recall (URGENT MEDICAL DEVICE ADVISORY)

FDA Classifies Voluntary Physician Advisory Letter on Riata and Riata ST Silicone Defibrillation Leads as Class I Recall (URGENT MEDICAL DEVICE ADVISORY)
Photos

 Riata Defibrillation Lead Label

Riata ST Defibrillation Lead Label

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