This is what I found on Web MD:
The U.S. Food and Drug Administration on Tuesday announced a ban on the sale of all pelvic mesh products.
The surgical mesh is typically used to repair pelvic organ prolapse (POP) and incontinence, but reported side effects have included permanent incontinence, severe discomfort and an inability to have sex.
“In order for these mesh devices to stay on the market, we determined that we needed evidence that they worked better than surgery without the use of mesh to repair POP,” said Dr. Jeffrey Shuren, director of the FDA’s Center for Devices and Radiological Health. “That evidence was lacking in these premarket applications, and we couldn’t assure women that these devices were safe and effective long term.”
Simply put, the remaining makers of the mesh devices — Boston Scientific and Coloplast — failed to prove the long-term safety or benefit of their devices, the FDA said in a news release.
The companies will have 10 days to submit plans to withdraw these products from the market, the FDA said. Most pelvic mesh products have already been taken off the market, according to the Associated Press.
Information provided by Web MD.
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