Lumenis VersaCut Tissue Morcellator: Class 1 Recall
MedSun: Newsletter #82, March 2013
FDA MedWatch Safety Alert
Lumenis Limited is recalling certain models of VersaCut Morcellator devices to correct its labeling. There is a potential for air embolisms to occur if the aspiration tubing is hooked up backwards to the aspiration control box housing.
Lumenis VersaCut Tissue Morcellator: Class 1 Recall. February 25, 2013.