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Medical Device Recall Rates Depend on Inspection Rotations

Research conducted by a team from Indiana University, University of Wisconsin, and University of Minnesota considered the impact of inspection rotations on recalls. The team looked at seven years of data in conducting the study, examining medical device recalls from over two thousand U.S. manufacturers. The research team sought to understand the impact of regulatory » Read More

Potential Risks in New Olympus Power Morcellator Study

In 1995, the Food and Drug Administration approved the laparoscopic power morcellator, a tool for OB/GYN surgeons to use in the removal of uterine fibroids. After Dr. Amy Reed of Philadelphia underwent a hysterectomy in 2013, she developed a uterine sarcoma. She and her husband, Dr. Hooman Noorchashm, discovered fabricated studies and increased cancer risks » Read More