BEUDAMED
    FDA Adverse Event Injury Summary report: N

    J LOOP POSTERIOR CHAMBER

    MDR report key: 13810 · Received January 26, 1994

    Report

    Report Number
    13810
    Event Type
    Injury
    Date Received
    January 26, 1994
    Date of Event
    July 8, 1993
    Report Date
    January 14, 1994
    Manufacturer
    ALCON SURGICAL, INC.
    Product Code
    HQL
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    LENS DISLOCATED THROUGH INFERIOR CAPSULAR HOLD 7 YRS AFTER INSERTION. REMOVED AND REPLACED WITH AC LENS. AC LENS HAPTIC FELL INTO IRIDECTOMY. REPOSITIONED 2 WEEKS AFTER ORIGINAL SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 J LOOP POSTERIOR CHAMBER Implant INTRAOCULAR LENS HQL ALCON SURGICAL, INC. 501

    Patients

    Seq Age Sex Outcome Treatment
    1 69 YR Required Intervention