BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 1974589 · Received December 29, 2010

    Report

    Report Number
    1831750-2010-05276
    Event Type
    Malfunction
    Date Received
    December 29, 2010
    Date of Event
    December 1, 2010
    Report Date
    December 1, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SLEEVE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE IS A WARPED SLEEVE. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED AC POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 3002S3 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK