Archive for the ‘Defibrillator Defects’ Category

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Several Brands of Automated External Defibrillators (AEDs) Recalled

By cwtelfair on March 5, 2012   /   Defibrillator Defects, Medical Device Defects, Product Liability   /   Leave a comment
Cardiac Science Powerheart AED

The U.S. Food and Drug Administration (FDA) has contacted medical professionals and health care organizations of a Class 1 recall for several models and brands of Automated External Defibrillators (AEDs). AEDs are used to treat victims with signs of cardiac arrest who are not breathing and are

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Class 1 Recall of St. Jude Medical Defibrillators

By cwtelfair on January 4, 2012   /   Defibrillator Defects, Medical Device Defects, Product Liability   /   Leave a comment

The U.S. Food and Drug Administration (FDA) has notified healthcare professionals of a Class 1 recall involving the St. Jude Medical Riata and Riata ST Silicone Endocardial Defibrillation Leads. The silicone based insulation covering the defibrillator leads is at risk of premature abrasion. When this abrasion occurs,

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