BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENU (UNKNOWN TYPE)

    MDR report key: 1040596 · Received May 9, 2008

    Report

    Report Number
    1313525-2008-00016
    Event Type
    Injury
    Date Received
    May 9, 2008
    Date of Event
    April 15, 2006
    Report Date
    April 11, 2008
    Manufacturer
    BAUSCH & LOMB
    Product Code
    LPN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PER THE ALLEGATIONS THE PLAINTIFF SUSTAINED SERIOUS AND PERMANENT INJURIES. THE CLAIM ALSO ALLEGES THAT THE PLAINTIFF HAS SUSTAINED LOSS OF HIS PHYSICAL ABILITIES AND FACULTIES. PATIENT CLAIMS TO HAVE USED RENU CONTACT LENS SOLUTION (UNKNOWN TYPE). NO ADDITIONAL INFORMATION IS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENU (UNKNOWN TYPE) 86LPN LPN BAUSCH & LOMB

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention