1. Medical devices: cancer risk led FDA to warn against certain uses of power morcellators and recommend new labeling : report to Congressional requesters Publication: Washington, D.C. : U.S. Government Accountability Office, February 2017 Subject(s): Device ApprovalEquipment SafetyMorcellation -- adverse effectsMorcellation -- instrumentationProduct LabelingLeiomyoma -- surgeryUterine Neoplasms -- surgeryHumansUnited StatesUnited States. Food and Drug Administration
2. Product labeling for certain ultrasonic surgical aspirator devices: guidance for Industry and Food and Drug Administration staff Publication: [Silver Spring, Maryland] : Center for Devices and Radiological Health, October 30, 2017 Subject(s): Product Labeling -- standardsUltrasonic Surgical Procedures -- instrumentationUltrasonic Surgical Procedures -- standardsEquipment Safety -- standardsLeiomyoma -- surgerySuction -- instrumentationSuction -- standardsSurgical Equipment -- adverse effectsUltrasonic Surgical Procedures -- adverse effectsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
