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.

Additional Information:

Lumenis VersaCut Tissue Morcellator: Class 1 Recall. February 25, 2013.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm340976.htm


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