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Drs. Miklos and Moore Respond to FDA Mesh Safety Communication

FDADrs. Miklos and Moore have written a response to the FDA Safety Communication released on July 13, 2011, regarding the usage of synthetic mesh materials for the repair of pelvic organ prolapse. While the FDA has neither taken the mesh off the market nor called for a recall, they did state that a variety of complications have been reported by patients and surgeons alike, and wish to make this fact known to surgeons and patients alike.

Drs. Miklos and Moore have a record of treating complications as a result of mesh surgery, and have also been pioneers and educators in their use. While it is impossible for any procedure to be entirely free of risk, Drs. Miklos and Moore have found the developed specific techniques for the usage of mesh which have greatly helped reduced complications and produce outcomes.

To read Dr. Miklos and Moore's complete response please click here.

To read the 13 questions the FDA suggests patients to ask their surgeons, click here.

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