BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BED

    MDR report key: 17527158 · Received August 12, 2023

    Report

    Report Number
    MW5134092
    Event Type
    Malfunction
    Date Received
    August 12, 2023
    Report Date
    February 17, 2012
    Manufacturer
    UNKNOWN
    Product Code
    FNL
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    ON JANUARY 25, 2012, STRYKER MEDICAL WAS NOTIFIED OF A POTENTIALLY REPORTABLE COMPLAINT INVOLVING A PRODUCT FOR WHICH STRYKER IS NOT THE MANUFACTURER. THE CUSTOMER REPORTED A POWER CORD WITH A PLUG HOUSING THAT DID NOT MAKE CONTACT WITH THE BED. PLEASE FIND ADDITIONAL CONTACT INFORMATION BELOW. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2182572 BED BED, AC-POWERED ADJUSTABLE HOSPITAL FNL UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown