BEUDAMED
    FDA Adverse Event Summary report: N

    ALCON 30 DEG TIP 316-1179-502

    MDR report key: 9759 · Received August 2, 1993

    Report

    Report Number
    9759
    Date Received
    August 2, 1993
    Report Date
    July 27, 1993
    Manufacturer
    ALCON SURGICAL, INC.
    Report Source
    User Facility report

    Narratives

    Description of Event or Problem · 1

    CATARACT EXTRACTION PROCEDURE WAS BEING PERFORMED. INTRAOPERATIVELY METAL APPEARING FRAGMENTS APPEARED IN EYE.INVALID DATA - REGARDING SINGLE USE LABELING OF DEVICE. PATIENT MEDICAL STATUS PRIOR TO EVENT: INVALID DATA. INVALID DATA - REGARDING MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE. NO DATA - REGARDING DATE LAST SERVICED. SERVICE PROVIDED BY: INVALID DATA. INVALID DATA - SERVICE RECORDS AVAILABILITY.INVALID DATA - REGARDING WHETHER EVENT PRESENTS IMMINENT HAZARD. INVALID DATA - WHETHER DEVICE USED AS LABELED/INTENDED.INVALID DATA - REGARDING EVALUATION BY USER AFTER EVENT. METHOD OF EVALUATION: INVALID DATA. RESULTS OF EVALUATION: INVALID DATA. CONCLUSION: INVALID DATA. CERTAINTY OF DEVICE AS CAUSE OF OR CONTRIBUTOR TO EVENT: INVALID DATA. CORRECTIVE ACTIONS: NO DATA. INVALID DATA - ON DEVICE DESTROYED/DISPOSED OF STATUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALCON 30 DEG TIP 316-1179-502 CATARACT EXTRACTION UNIT ALCON SURGICAL, INC. ALCON 30 DEG TIP 316-1179-502 92241

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Invalid Data