The evidence against metal-on-metal hip implants continues to grow. Late last month, a joint report from the BBC and the British Medical Journal indicated that recipients of large...
Ever since DePuy Orthopaedics, a division of Johnson & Johnson, recalled nearly 93,000 of their ASR metal-on-metal hip implant devices in August of 2010 there has been a near constant...
A detailed review of safety studies caused the U.S. Food and Drug Administration (FDA) to reject Johnson & Johnson’s sale of an artificial hip in the U.S., but it didn’t stop the company from...
Following up on previous warnings about the safety of transvaginal mesh implants to treat pelvic organ prolapse, the FDA is now enlisting the research power of the manufacturers of these devices....
The FDA is reclassifying the surgical mesh implant devices in a higher risk category in order to require manufacturers to conduct clinical trials on people before receiving approval of the...
As the DePuy recalled hip replacement device lawsuits are entering into the money phase of the lawsuit cycle, insurance companies are beginning to make claims for the patients’ portion of...
Hip implant complaints are surging as more information is revealed about the dangers of metal on metal hip joint devices. Recent studies show that the FDA received more than 5,000 reports since...
Many women who have experienced complications following transvaginal mesh surgery have suffered as a result of a bad product being surgically placed inside of their bodies. There have been a...
The U.S. Food and Drug Administration (FDA) recently issued a warning regarding vaginal surgeries that use mesh to repair pelvic organ prolapse. According to the warning, the procedures are no...
Each year, more than 200,000 women undergo surgery for pelvic organ prolapse (POP). Pelvic organ prolapse is a medical condition that occurs when the normal support of the vagina is lost,...
Showing items 1 to 10 of 44
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