Sorin Group USA, Inc.: Medical Device Recalls in 2013

According to to data from the FDA, there were 2 medical device recalls made by Sorin Group USA, Inc. in 2013. See the details of the recalls below.

You can see similar recalls for other firms.

• Isoline Implantable Defibrillation Lead, Model Isoline 2CR5, 2CR6 and 2CT6. These lead models are indicated for ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life threatening arrhythmias
• Edwards Lifesciences Suction Wand Model S099B, packaged in Sorin Group Heart/Lung Perfusion Packs.