Unknown Saline Implants

Description of Event or Problem

It was reported that a 50-year-old Caucasian female patient underwent revision breast augmentation with unknown size Unknown Saline Implants and experienced breast implant deflation on her right side postoperatively. As a result, the patient is scheduled for surgery on (b)(6)2026.

Additional Manufacturer Narrative

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.Since no lot number was provided, no manufacturing record evaluation could be performed.Reason for device explant and/or reoperation: Right Deflation.D4: UDI: As the catalog/model number was not provided, the (01)GTIN is not available.D4: UDI: As the lot, serial number, and corresponding expiration date for the device involved in the event was not provided, the full UDI is currently not available.D6b Explanation Date: (b)(6) 2026.Mentor is submitting this report pursuant to the provisions of 21 CFR, Part 803. This report may be based on information which Mentor has not been able to investigate or verify prior to the required reporting date. This report does not reflect a conclusion by FDA, Mentor, or its employees that the report constitutes an admission that the device, Mentor, or its employees caused or contributed to the potential event described in this report. Manufacturer¿s reference number:(b)(4).