BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PIPETTING ASSEMBLY (W/GLASS SYRINGE)

    MDR report key: 3032907 · Received March 29, 2013

    Report

    Report Number
    1213649-2013-00009
    Event Type
    Malfunction
    Date Received
    March 29, 2013
    Date of Event
    October 9, 2012
    Report Date
    October 9, 2012
    Manufacturer
    CADENCE INC.
    Product Code
    FMF
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    CADENCE ACKNOWLEDGES THIS REPORT DOES NOT MEET THE THIRTY DAY REPORTING REQUIREMENTS. THIS WAS UNINTENTIONAL. THIS REPORT IS BEING FILED AFTER IT WAS IDENTIFIED AS NON-COMPLAINT DURING AN INTERNAL REVIEW OF OUR COMPLAINT FILES.

    Description of Event or Problem · 1

    ON (B)(6) 2012, THE CUSTOMER REPORTED THE GLASS SYRINGE WAS FOUND BROKEN WHEN THE BOX WAS OPENED. THERE WAS NO PATIENT EXPOSURE AND NO INJURY TO THE USER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    130660 PIPETTING ASSEMBLY (W/GLASS SYRINGE) SYRINGE FMF CADENCE INC. 5710 82077-01

    Patients

    Seq Age Sex Outcome Treatment
    1 Other