BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUICKSET TPRD HEX SCDR CARDAN

    MDR report key: 8841100 · Received July 30, 2019

    Report

    Report Number
    1818910-2019-99637
    Event Type
    Malfunction
    Date Received
    July 30, 2019
    Date of Event
    July 12, 2019
    Report Date
    July 11, 2019
    Manufacturer
    DEPUY ORTHOPAEDICS, INC. 1818910
    Product Code
    HXX
    UDI-DI
    10603295109259
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH DEPUY SYNTHES HAS NOT BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY FDA, DEPUY SYNTHES OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE DEVICE, DEPUY SYNTHES, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. PRODUCT COMPLAINT # (B)(4). EXAMINATION OF THE RETURNED INSTRUMENT CONFIRMED THE REPORTED OBSERVATION. THE ROOT CAUSE IS ATTRIBUTED TO DESIGN. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY. DEVICE HISTORY LOT : NULL. DEVICE HISTORY BATCH : NULL. DEVICE HISTORY REVIEW : NULL. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

    Additional Manufacturer Narrative · 1

    PRODUCT COMPLAINT # (B)(4). IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WE LOST BUSINESS, A LOT OF BUSINESS HERE IN TOWN. ALL INSTRUMENTS HAVE BEEN PULLED TO RE-ALLOCATE WITHIN OUR TERRITORY. BROKEN INSTRUMENTS WERE IN DESIGNATED BOX AT FACILITY LABELED AS "BROKEN" OR WERE FOUND IN STERILE WRAPPED SETS THAT WERE RETURNED TO THE OFFICE. NO PATIENT WAS AFFECTED. NO SURGERY WAS AFFECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    636151 QUICKSET TPRD HEX SCDR CARDAN HIP INSTRUMENTS : SCREWDRIVERS HXX DEPUY ORTHOPAEDICS, INC. 1818910 A0210 10603295109259

    Patients

    Seq Age Sex Outcome Treatment
    1