BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIME CARE (R) TRANSCEND MATTRESS

    MDR report key: 4190177 · Received September 18, 2014

    Report

    Report Number
    3007538326-2014-00095
    Event Type
    Malfunction
    Date Received
    September 18, 2014
    Date of Event
    August 22, 2014
    Report Date
    September 16, 2014
    Manufacturer
    PRIMUS MEDICAL LLC
    Product Code
    IKY
    Removal / Correction Number
    Z-2596-2014
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS MATTRESS HAS NOT BEEN INSPECTED AND THE LOT NUMBER HAS NOT BEEN DOCUMENTED YET DUE TO THE MATTRESS NOT BEING RETURNED. THE FIRM WILL BE SWITCHING OUT MATTRESSES AT THE FACILITY ON (B)(6) 2014. THIS PROBLEM HAS BEEN ASSIGNED TO CAPA # (B)(4), AND A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE CORRECTIVE ACTION.

    Description of Event or Problem · 1

    UPON RECEIPT OF THE RECALL PACKET THE CUSTOMER NOTIFIED THE FIRM THEY HAD A DELAMINATED MATTRESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    577603 PRIME CARE (R) TRANSCEND MATTRESS IKY PRIMUS MEDICAL LLC TCM4280

    Patients

    Seq Age Sex Outcome Treatment
    1