BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LD304 MATERNITY BED

    MDR report key: 1851289 · Received September 22, 2010

    Report

    Report Number
    1831750-2010-02519
    Event Type
    Malfunction
    Date Received
    September 22, 2010
    Date of Event
    August 30, 2010
    Report Date
    September 7, 2010
    Manufacturer
    STRYKER CORP. MEDICAL DIVISION
    Product Code
    HDD
    PMA / PMN Number
    K950889
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    EI
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: MANUAL CPR RELEASE.

    Description of Event or Problem · 1

    IT WAS REPORTED VIA A SERVICE REPORT THAT, THE FOWLER WOULD NOT GO UP OR DOWN INTERMITTENTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LD304 MATERNITY BED LABOR AND DELIVERY BED HDD STRYKER CORP. MEDICAL DIVISION 4701 NA

    Patients

    Seq Age Sex Outcome Treatment
    1