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Press Releases:

» (11/11/09 ) Medicare Should Deny Payment for Unproven Anti-Depression Device » (9/25/09 ) Medicare Should Deny Payment for Knee Device That FDA Improperly Approved » (9/24/09 ) FDA Internal Review Slams Knee Device’s Approval Process » (3/13/09 ) Defibrillator Recall Raises More Concerns About FDA’s Competency » (3/10/09 ) FDA Negligent in Delayed Response to Problems With Pediatric Breathing Device » (3/9/09 ) FDA’s Approval of Anti-Scarring Device for Children Is Another in Long Line of Questionable Decisions » (3/6/09 ) Medical Device Maker’s Brazen Manipulation Of Approval Process Shows Need to Reform FDA » (1/15/09 ) GAO Report Documents Lax Device Approval Standards at FDA » (11/13/08 ) FDA Support of Heart Device Would Fly in Face of Sound Science » (2/6/07 ) Medicare Right to Reject Brain Stimulation Device » (11/17/06 ) Silicone Gel Breast Implants: Most Defective Medical Device Ever Approved by the FDA » (9/6/06 ) Medicare Should Not Reimburse for Implantable Vagus Nerve Stimulation Device for Depression » (9/14/05 ) Potentially Harmful Medical Devices Should Be Recalled When Safer Alternatives Are Developed, Public Citizen Tells FDA » (7/18/05 ) Approval of Device to Treat Depression Is One of Most Questionable FDA Decisions in Recent Memory » (5/11/05 ) Electronic Device Should Not Be Approved for Treatment of Depression, Public Citizen Tells FDA » (1/8/04 ) Statement of Sidney M. Wolfe, M.D. Director, Public Citizen’s Health Research Group, Concerning FDA Non-Approvable Letter for Silicone Gel Breast Implants » (10/14/03 ) Approval of Silicone Gel Breast Implants Based on Only Three Years of Data Would Be Foolhardy, Public Citizen Tells FDA » (8/25/03 ) Health and Advocacy Groups Call on U.S. FDA to Halt Breast Implant Approval Process

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