Public Citizen demands recall of surgical mesh
The watchdog group, Public Citizen, has strongly urged the US Food & Drug Administration to recall surgical mesh used in patients with pelvic organ prolapse. The consumer advocacy group argues that the mesh product, made by Minneapolis-based Coloplast and American Medical Systems Inc., exposes women to serious risks and possibly permanent damage.
Nearly 300,000 women a year undergo surgery where surgical mesh is used. Public Citizen says they believe at least 75,000 people have potentially dangerous mesh surgically implanted in their bodies. The FDA had issued a warning for the product last month, but the watchdog group wants the FDA to issue a full recall.
If you or a loved one has been injured due to a defective, malfunctioning, or otherwise dangerous product, contact the Minnesota product liability lawyers of Robert Wilson & Associates at (612) 334-3444.