BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUPER SUCKER SHORT CURVED (BX/20)

    MDR report key: 3966914 · Received December 9, 2013

    Report

    Report Number
    1045834-2013-14490
    Event Type
    Malfunction
    Date Received
    December 9, 2013
    Date of Event
    August 10, 2012
    Report Date
    August 15, 2012
    Manufacturer
    DEPUY SYNTHES POWER TOOLS
    Product Code
    KDC
    PMA / PMN Number
    K822065
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE WAS RECEIVED BY DEPUY SYNTHES POWER TOOLS. THE DEVICE WAS EVALUATED AND THE CUSTOMER'S COMPLAINT OF PACKAGING DEFECTS COULD NOT BE CONFIRMED. VISUAL INSPECTION ACCEPTANCE CRITERIA ARE "NO LOOSE FOREIGN MATERIAL (LFM) WHEN INSPECTED AT (B)(4) MAGNIFICATION." NO LFM COULD BE FOUND ON THE DEVICE WHEN INSPECTED AT (B)(4) MAGNIFICATION. ALSO, THE PACKAGE IS IN GOOD CONDITION WITH NO DEFECTS OF THE PEELABLE OR TERMINAL SEAL. IF ADD'L INFO BECOMES AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SENT.

    Description of Event or Problem · 1

    REPORT 12 OF 25. REPORT RECEIVED FROM (B)(6) STATING THE DEVICE "FAILED DISTRIBUTOR'S INSPECTION." IT IS KNOWN THAT THIS EVENT DID NOT OCCUR DURING SURGERY AND THAT THERE WAS NO PT/USER INJURY OR MEDICAL INTERVENTION. THERE WAS NO ADD'L INFO PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    637771 SUPER SUCKER SHORT CURVED (BX/20) KDC DEPUY SYNTHES POWER TOOLS F073061273

    Patients

    Seq Age Sex Outcome Treatment
    1