BEUDAMED
    FDA Adverse Event Other Summary report: N

    STRYKER BIRTHING BED

    MDR report key: 511983 · Received February 13, 2004

    Report

    Report Number
    1831750-2004-00002
    Event Type
    Other
    Date Received
    February 13, 2004
    Date of Event
    December 20, 2003
    Report Date
    January 14, 2004
    Manufacturer
    STRYKER CORP, MEDICAL DIV
    Product Code
    HDD
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A PT WAS BEING TRANSPORTED ON THE DELIVERY BED. ALLEGEDLY, ONE NURSE WAS MOVING THE BED WHILE ANOTHER NURSE WAS HOLDING THE FOOT SECTION ON THE BED WHICH WAS NOT LATCHED IN PLACE. IT WAS REPORTED THAT DURING THE TRANSPORT THE BED RAN OVER THE TOES OF THE NURSE HOLDING THE FOOT SECTION ALLEGEDLY FRACTURING THEIR TOES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER BIRTHING BED BIRTHING BED HDD STRYKER CORP, MEDICAL DIV 5010 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention