December 28, 2016 By The U.S. Food and Drug Administration Greatbatch Medical Recalls Standard Offset Cup Impactor Used for Hip Joint Replacement due to Inadequate Sterilization
December 22, 2016 By The U.S. Food and Drug Administration FDA Permits Marketing of New Tissue Expander for Women Undergoing Breast Reconstruction Following Mastectomy
December 14, 2016 By The U.S. Food and Drug Administration FDA Approves First Autologous Cellularized Scaffold for the Repair of Cartilage Defects of the Knee
December 8, 2016 By The U.S. Food and Drug Administration FDA Takes Steps to Improve Hearing Aid Accessibility
November 30, 2016 By The U.S. Food and Drug Administration Cochlear Implants: A Different Kind of ‘Hearing’
November 30, 2016 By The U.S. Food and Drug Administration HeartWare Recalls Ventricular Assist Device Pumps Due to Contamination Causing Electrical Issues
November 30, 2016 By The U.S. Food and Drug Administration SentreHeart Recalls FindrWIRZ Guidewire System due to Coating Separation