(b)(4).Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the device remains implanted.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Concomitant medical products: item # 00430008700, glenoid component pegged 52 mm diameter articular surface used with blue (52 mm) instruments, lot # 61626329 item # 00430205219, offset modular humeral head 19 mm head height 52 mm spherical head diameter, lot # 61966672.Reported by patient.Multiple mdr reports were filed for this event, please see associated reports: 0001822565 - 2018 - 05737, 0001822565 - 2018 - 05738.
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It was reported that following removal of a fractured cerclage wire, the patient experienced the formation of hematoma approximately twelve (12) days post-op.During follow-up visits approximately three (3) weeks and two (2) months after the cerclage wire removal, the hematoma was smaller and the patient had full range of motion of shoulder.However, the patient is still experiencing some ongoing shoulder pain.Attempts have been made and no further information has been provided.
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