Since the device has not been returned for analysis, no product failure analysis can be conducted, and no determination of possible contributing factors can be made. As such, the investigation will be closed. If the complaint device is received in the future, the investigation will be reopened and conducted as appropriate. A manufacturing record evaluation is in progress. Once completed, a supplemental report will be submitted. Reason for device explant and/or reoperation: rupture. Manufacturer? S reference number: (b)(4).
Patient Sequence No: 1, Text Type: N, H10
It was reported that a (b)(6) year-old african american female patient underwent a breast augmentation revision with mentor memorygel breast implants 350cc and experienced bilateral rupture. As a result, the patient is scheduled for removal on (b)(6) 2020 this report is for the left breast prosthesis.
Patient Sequence No: 1, Text Type: D, B5