BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MULLER AWL REAMER W/HUDSON END

    MDR report key: 9885413 · Received March 26, 2020

    Report

    Report Number
    1818910-2020-09413
    Event Type
    Malfunction
    Date Received
    March 26, 2020
    Date of Event
    March 13, 2020
    Report Date
    March 13, 2020
    Manufacturer
    DEPUY ORTHOPAEDICS INC US
    Product Code
    HWE
    UDI-DI
    10603295119821
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISION OF 21 CFR, PART 803. THE REPORT MAY BE BASED ON THE 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). INVESTIGATION SUMMARY: THE DEVICE WAS REVIEWED BY DEPUY ENGINEERING MELBOURNE IN A-3963976 WHICH STATES MY ASSESSMENT IS THAT THIS COMPLAINT IS DUE TO WEAR AND TEAR. ROOT CAUSE ATTRIBUTED TO THE DEVICE BEING WORN FROM NORMAL USE AND SERVICING. DEPUY SYNTHES CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION MAY BE RE-OPENED AS NECESSARY. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

    Additional Manufacturer Narrative · 0

    PRODUCT COMPLAINT # (B)(4). INVESTIGATION SUMMARY THE DEVICE WAS REVIEWED BY DEPUY ENGINEERING MELBOURNE IN (B)(4) WHICH STATES MY ASSESSMENT IS THAT THIS COMPLAINT IS DUE TO WEAR AND TEAR. ROOT CAUSE ATTRIBUTED TO THE DEVICE BEING WORN FROM NORMAL USE AND SERVICING. DEPUY SYNTHES CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION MAY BE RE-OPENED AS NECESSARY. DEVICE HISTORY LOT NULL DEVICE HISTORY BATCH NULL DEVICE HISTORY REVIEW NULL.

    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

    T HANDLE CRACKED AND REAMER BLUNT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    348491 MULLER AWL REAMER W/HUDSON END HIP INSTRUMENTS : REAMERS HWE DEPUY ORTHOPAEDICS INC US 2354-10-000 A1005 10603295119821

    Patients

    Seq Age Sex Outcome Treatment
    1