(b)(4).Attempts are being made to obtain the following information.To date no response has been provided.If further details are received at a later date a supplemental medwatch will be sent.The patient demographic info: age, weight, bmi at the time of index procedure date and name of initial surgical procedure the diagnosis and indication for the initial surgical procedure? what are the patient comorbidities/concomitant medications? the initial approach for the index surgical procedure? any concurrent procedure/device implantation? were there any intra-operative complications? when was the mesh exposure first noted by a physician? mesh exposure diagnostic confirmation? when did the bleeding occur? the source and triggering event of bleeding and the volume of blood loss? describe any medical/surgical intervention for exposure/bleeding including dates and surgical findings.Was any abnormality of the device noted prior to, during or after the procedure? product code and lot # what is physicians opinion as to the etiology of or contributing factors to this event? what is the patient's current status?.
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