The patient was reportedly implanted with an ethicon gynecare secur and a surgisis product on (b)(6) 2007, by dr.(b)(6).The patient was implanted with a boston scientific pinnacle pelvic floor repair kit on (b)(6) 2008, by dr.(b)(6) and dr.(b)(6).Both surgeries took place at (b)(6).The patient and her attorney have alleged that as a result of these products 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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