BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE ACUTE CARE BED 3/01

    MDR report key: 1933085 · Received December 13, 2010

    Report

    Report Number
    1831750-2010-04766
    Event Type
    Malfunction
    Date Received
    December 13, 2010
    Date of Event
    November 16, 2010
    Report Date
    November 16, 2010
    Manufacturer
    STRYKER CORP.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION: CUSTOMER WAS GIVEN THE PART NUMBERS THAT THEY NEEDED TO FIX THE PARTS THAT NEEDED REPLACEMENT.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT TECH WAS REQUESTED TO STOP BY BECAUSE OF A PARTS PROBLEMS. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE ACUTE CARE BED 3/01 A/C POWERED HOSPITAL BED FNL STRYKER CORP. 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1