BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MENTOR MEMORYGEL BREAST IMPLANT

    MDR report key: 18567348 · Received January 23, 2024

    Report

    Report Number
    1645337-2024-00842
    Event Type
    Injury
    Date Received
    January 23, 2024
    Date of Event
    December 6, 2023
    Report Date
    January 23, 2024
    Manufacturer
    MENTOR TEXAS
    Product Code
    FTR
    UDI-DI
    00081317000273
    PMA / PMN Number
    P030053
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    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 (MRE) WAS PERFORMED, AND NO ANOMALIES WERE FOUND RELATED TO THIS COMPLAINT. IN ADDITION, THE MRE VERIFIES THAT THE DEVICE WAS MANUFACTURED IN ACCORDANCE WITH DOCUMENTED SPECIFICATION AND PROCEDURES. REASON FOR DEVICE EXPLANT AND/OR REOPERATION: ANISOMASTIA. 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).

    Description of Event or Problem · 0

    IT WAS REPORTED THAT A PATIENT UNDERWENT PRIMARY BREAST AUGMENTATION WITH TWO 275CC MENTOR MEMORYGEL BREAST IMPLANTS. POST-OPERATIVELY, THE PATIENT WANTED TO UPGRADE TO BIGGER BREAST IMPLANTS AND ALSO SUFFERED FROM BILATERAL BREAST CAPSULAR CONTRACTURES (BAKER GRADE 2-3 ON THE RIGHT AND BAKER GRADE 1 ON THE LEFT). AS A RESULT, THE PATIENT UNDERWENT BILATERAL BREAST IMPLANT REMOVAL AND REPLACEMENT SURGERY ON (B)(6) 2023. DURING THE REMOVAL SURGERY, A SUPERIOR CAPSULOTOMY AND CAPSULECTOMY WERE PERFORMED ON THE LEFT BREAST TO GET THE IMPLANT TO SIT LOWER. THE RIGHT BREAST IMPLANT WAS DISCOVERED TO BE RUPTURED. ANOTHER SUPERIOR CAPSULOTOMY WAS PERFORMED ON THE RIGHT BREAST SINCE IT WAS TIGHT AND AN ANTERIOR ONE WAS PERFORMED DUE TO SLIGHT CONTOUR INDENTATION. SUBSEQUENTLY, BOTH THE IMPLANTS WERE REPLACED WITH THE FOLLOWING DEVICES: (RIGHT) 310CC MENTOR MEMORYGEL XTRA BREAST IMPLANT CATALOG: SMHX310 LOT: 9812881 SN: (B)(6) AND (LEFT) 310CC MENTOR MEMORYGEL XTRA BREAST IMPLANT CATALOG: SMHX310 LOT: 9597506 SN: (B)(6). THIS MEDWATCH FORM IS FOR THE LEFT BREAST PROSTHESIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1533298 MENTOR MEMORYGEL BREAST IMPLANT PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED FTR MENTOR TEXAS 5806582 00081317000273

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Female Required Intervention