BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HYDROVIEW INTRAOCULAR LENS

    MDR report key: 459689 · Received May 12, 2003

    Report

    Report Number
    1920664-2003-00275
    Event Type
    Malfunction
    Date Received
    May 12, 2003
    Date of Event
    March 27, 2003
    Report Date
    April 14, 2003
    Manufacturer
    BAUSCH & LOMB
    Product Code
    HQL
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    DEPOSITS ON THE LENS SURFACE HAVE BEEN NOTICED. DATE OF ORIGINAL SURGERY 02/1998. THE PATIENT VISUAL ACUITY IS 20/30.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HYDROVIEW INTRAOCULAR LENS INTRAOCULAR LENS HQL BAUSCH & LOMB NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN