BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1213643-1999-00061

    MDR report key: 257105 · Received December 29, 1999

    Report

    Report Number
    1213643-1999-00061
    Event Type
    Malfunction
    Date Received
    December 29, 1999
    Date of Event
    December 25, 1999
    Report Date
    December 28, 1999
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    UNABLE TO TRANSFER BLOOD FROM COLLECTION CHAMBER TO REINFUSION BAG.

    Patients

    Seq Age Sex Outcome Treatment
    1 *