BEUDAMED
    FDA Adverse Event Other Summary report: N

    BREAST IMPLANT (RIGHT)

    MDR report key: 24427788 · Received February 23, 2026

    Report

    Report Number
    MW5184259
    Event Type
    Other
    Date Received
    February 23, 2026
    Report Date
    February 13, 2026
    Manufacturer
    UNKNOWN
    Product Code
    FTR
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    IN COMPLIANCE WITH MDR REPORTING REGULATION, SECTION 803.22, WE WISH TO INFORM YOU OF AN ADVERSE EVENT ASSOCIATED WITH ANOTHER MANUFACTURER'S DEVICE WHICH HAS BEEN RECEIVED AT ALLERGAN INC. ((B)(6) REF (B)(4)). ALLEGED EVENT: HEALTHCARE PROFESSIONAL REPORTED "CAPSULAR CONTRACTURE" OF A NON-(B)(6) DEVICE. THIS RECORD IS FOR THE LEFT SIDE. THE DEVICE WAS EXPLANTED. PATIENT CODE: 1761. DEVICE CODE: 4001. REFERENCE REPORT MW5184258. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    473481 BREAST IMPLANT (RIGHT) PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED FTR UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown