BEUDAMED
    FDA Adverse Event Other Summary report: N

    LD304 MATERNITY BED

    MDR report key: 1911535 · Received November 24, 2010

    Report

    Report Number
    1831750-2010-04196
    Event Type
    Other
    Date Received
    November 24, 2010
    Date of Event
    October 26, 2010
    Report Date
    October 26, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    HDD
    PMA / PMN Number
    K950889
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: SHIPPING DAMAGE. PRODUCT WAS BEING MOVED FROM A STORAGE LOCATION TO THE HOSPITAL FACILITY BY THE USER FACILITY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER LITTER TOP WAS DAMAGED/ BROKEN LITTER WELDMENT/ BROKEN LITTER TOP MID SECTION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1