The patient was reportedly implanted with an ams monarc subfascial hammock, an ams apogee with intepro lite, and an ams perigee with intepro lite on (b)(6) 2008 and a biodesign or surgisis vaginal erosion repair graft on (b)(6) 2009.Both surgeries took place at (b)(6) and were performed by dr.(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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