The U.S. Food and Drug Administration ordered the two makers of surgical mesh for women’s pelvic repair to take their products off the market, responding to years of complaints about pain, bleeding and scarring from the devices.
The federal agency, following a safety hearing on the topic in February, said that Boston Scientific Corp. and Coloplast Corp. hadn’t demonstrated reasonable evidence that the mesh products worked better than surgery without the products.
Who in their right mind would put plastic in their bodies?
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La FDA (Food Drog Administration) recibe informes elaborados por las propias empresas, ¿cómo es que esos mismos informes hacen desfavorables a sus productos? Véase la historia del espartamo.
Under the Trump administration you have to ask yourself if the FDA is getting any money for the approval?
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