BEUDAMED
    FDA Adverse Event Injury Summary report: N

    REGENT MEDICAL

    MDR report key: 372653 · Received January 14, 2002

    Report

    Report Number
    1065445-2002-00003
    Event Type
    Injury
    Date Received
    January 14, 2002
    Report Date
    January 14, 2002
    Manufacturer
    LRC HOSPITAL PRODUCTS, SDM
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ALLEGEDLY, A RESPIRATORY THERAPIST DEVELOPED A LATEX ALLERGY WHILE USING UNIDENTIFIED GLOVES. SSL AMERICAS, INC WAS NOTIFIED OF THE ALLEGED EVENT BY A PROCESS OF LITIGATION INVOLVING SEVERAL COMPANIES. IT IS UNCLEAR THAT THE CO'S DEVICE WAS USED OR CAUSE ANY INJURY TO THE PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REGENT MEDICAL LATEX GLOVES LYY LRC HOSPITAL PRODUCTS, SDM UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention