Cordis Optease Retrievable Inferior Vena Cava (IVC) Filter: Recall
MedSun: Newsletter #87, August 2013
FDA MedWatch Safety Alert
Cordis and FDA notified healthcare professionals and their organizations of a product labeling correction to provide clarification and additional information to minimize likelihood of implanting the filter backwards. This recall covers 33,000 units distributed in the United States between 05/06/2010 and 04/02/2013.
Cordis Optease Retrievable Inferior Vena Cava (IVC) Filter: Recall. FDA MedWatch Safety Alert. August 8, 2013.