- Medical Malpractice
- Product
- Unsafe Drugs
- Pradaxa
- Metal-on-Metal Hip Implant Litigation
- Hip Implants - DePuy ASR Hip Recall
- Hip Implants - Zimmer Durom Cup Hip Recall
- Vaginal Mesh Litigation
- Vaginal Mesh - Bard Avaulta Surgical Mesh
- Accutane
- Actos
- Avandia
- Bisphosphonate Litigation
- Chantix
- Darvon and Darvocet Recall
- Knee Implant - Zimmer NexGen CR-Flex
- Kugel Hernia Mesh Patches
- Mentor ObTape Vaginal Sling
- Ortho Evra Birth Control Patch
- Yasmin, Yaz, and Ocella Birth Control
- Other/Archive Drug Products
- Personal Injuries
- Auto Accidents
- Nursing Home Abuse
FDA Scientists complain of widespread FDA managerial misconduct to Obama transition team
A group of nine FDA scientists submitted a letter to the President-elect Obama transition team expressing frustration and outrage regarding the FDA’s scientific review process for medical devices and claim that the system of approving medical devices has been corrupted by current FDA managers. They claim in their letter that questionable medical devices are being approved putting public safety at risk and that, “Managers have ordered, intimidated and coerced FDA experts to modify scientific evaluations, conclusions and recommendations in violation of the laws.” The FDA has declined publicly to respond to the letter.
Click here to read entire Associated Press article from January 9, 2008
