BEUDAMED
    FDA Adverse Event Malfunction Summary report: Y

    11G CURETTE

    MDR report key: 16806635 · Received April 25, 2023

    Report

    Report Number
    0001811755-2023-00055
    Event Type
    Malfunction
    Date Received
    April 25, 2023
    Date of Event
    March 31, 2023
    Report Date
    April 25, 2023
    Manufacturer
    STRYKER INSTRUMENTS-KALAMAZOO
    Product Code
    OCJ
    UDI-DI
    07613252639794
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. REPORTED EVENTS: 1 EVENT WAS REPORTED FOR THIS QUARTER. PRODUCT RETURN STATUS: 1 DEVICE WAS NOT AVAILABLE FOR EVALUATION. ADDITIONAL INFORMATION: 1 DEVICE WAS LABELED FOR SINGLE-USE. 1 DEVICE WAS NOT REPROCESSED OR REUSED. H3 OTHER TEXT : DEVICE DISCARDED.

    Description of Event or Problem · 0

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT IN WHICH THE DEVICE OR CUTTING ACCESSORY FRACTURED. 1 EVENT HAD PATIENT INVOLVEMENT; NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    464760 11G CURETTE SPINAL CHANNELING INSTRUMENT, VERTEBROPLASTY OCJ STRYKER INSTRUMENTS-KALAMAZOO 0306621000 VMSR 07613252639794

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown