BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 1974097 · Received December 28, 2010

    Report

    Report Number
    1831750-2010-05264
    Event Type
    Malfunction
    Date Received
    December 28, 2010
    Date of Event
    November 30, 2010
    Report Date
    November 30, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    WALL OUTLET NOT FUNCTIONING. BED DID NOT HAVE A FAILURE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED EXIT IS NOT WORKING THERE IS RESPONDER 3, 4, & 5 IN THE HOSPITAL. THE NURSE CALL AND BED EXIT WORKS ON 4 AND 5 RESPONDER BUT NOT ON ALL OF THE 3. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP, MEDICAL DIVISION 3002S3EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1