BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZOOM CRITICAL CARE BED

    MDR report key: 1933260 · Received December 2, 2010

    Report

    Report Number
    1831750-2010-04350
    Event Type
    Malfunction
    Date Received
    December 2, 2010
    Date of Event
    November 2, 2010
    Report Date
    November 2, 2010
    Manufacturer
    STRYKER CORP. MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: TIMING LINK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE TIMING LINK NEEDED REPLACED ON THE SIDE RAIL. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT, NO ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZOOM CRITICAL CARE BED A/C POWERED HOSPITAL BED FNL STRYKER CORP. MEDICAL DIV. 2040 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK