European drug and medical device regulators have asked a scientific committee to review the safety of transvaginal mesh devices and whether the risks outweigh the benefits. The European Commission charged its Scientific Committee on Emerging and Newly Identified Health Risks to conduct the analysis on the surgical mesh products used to treat common pelvic floor disorders such as pelvic organ prolapse and stress urinary incontinence. The request is based on mounting reports of injuries associated with the devices, which range in severity and include complications such as rejection, tissue erosion, mesh exposure and shrinkage resulting in symptoms such as chronic ... Read More
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