The patient was reportedly implanted with a biodesign or surgisis urethral sling and a biodesign or surgisis posterior pelvic floor graft on (b)(6)2012, at (b)(6) hospital in (b)(6), by dr.(b)(6).The patient and her attorney have alleged that as a result of these product being implanted in the patient, the patient has experienced pain, injury, and has undergone medical treatment.The following information was not provided by the complainant; specific information of the alleged injury.Specific information regarding whether intervention was performed.Specific information regarding why intervention was performed or what type/to what extent intervention was performed.Specific correlation between device performance and alleged injury.Current patient status.
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