BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STERIS AMSCO

    MDR report key: 225725 · Received June 3, 1999

    Report

    Report Number
    225725
    Event Type
    Injury
    Date Received
    June 3, 1999
    Date of Event
    May 25, 1999
    Report Date
    May 26, 1999
    Manufacturer
    STERIS CO.
    Product Code
    FLF
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    ETHYLENE CANISTER LEAKED IN "CSR". EMPLOYEE HAD ONE SPOT ON HER. NO INJURY TO THE EMPLOYEE. SEEN IN ER, NO KNOWN INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STERIS AMSCO ETO CANISTER FLF STERIS CO. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Life Threatening