BEUDAMED
    FDA Adverse Event Injury Summary report: N

    REGENEREX ACETABULAR SHELL 64ODX54ID

    MDR report key: 7752778 · Received August 6, 2018

    Report

    Report Number
    0001825034-2017-10872
    Event Type
    Injury
    Date Received
    August 6, 2018
    Date of Event
    February 12, 2016
    Report Date
    August 6, 2018
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    LPH
    PMA / PMN Number
    PK052996
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). FOREIGN: (B)(6). CONCOMITANT MEDICAL PRODUCTS: 22-301303, ARCOS CON SZ C STD 60MM HA, 682750; 22-300817, ARCOS 17X150MM SPL TPR DIST HA, 047050; XL-223654, HWAL ARCOMXL ALLPOLY 36IDX54OD ,710780; 650-0840, 36MM COCR BIOMET FEM HD -3 NK, 1524524; 103531, TI LOW PROFILE SCREW 6.5X20MM, 3187124; 103531, TI LOW PROFILE SCREW 6.5X20MM, 3147716; 103533, TI LOW PROFILE SCREW 6.5X30MM, 2915874; 103536, TI LOW PROFILE SCREW 6.5X45MM, 2846235; UNKNOWN CERCLAGE WIRES. THE COMPLAINT CAN BE CONFIRMED BASED ON THE INFORMATION PROVIDED FROM THE CLINICAL STUDY AND X-RAYS. THE X-RAY REVIEW SHOWS OVERALL FIT AND ALIGNMENT OF THE IMPLANT IS APPROPRIATE. NO OBVIOUS SIGNS OF LOOSENING OR RADIOLUCENCY SEEN ON THESE IMAGES. RADIOLOGIST NOTED A PROXIMAL CERCLAGE WIRE IS FRACTURED ON THE 1 YR & 3 YR IMAGE. RADIOLOGIST NOTES PERSISTENT FRACTURE INVOLVING THE PROXIMAL LEFT FEMORAL DIAPHYSIS ON IMMEDIATE POST OP AND 3 YR IMAGE. DEVICE HISTORY RECORDS REVIEWED AND IDENTIFIED NO DEVIATIONS OR ANOMALIES THAT COULD LEAD TO THE REPORTED EVENT. A DEFINITIVE ROOT CAUSE CANNOT BE PROVIDED BASED ON THE INFORMATION PROVIDED. THE WIRE FRACTURE AND DIAPHYSIS FRACTURE COULD BE CONTRIBUTING FACTORS TO THE REPORTED PATIENT¿S CONDITION. IT IS UNCONFIRMED IF THE FRACTURE IS A NONUNION OF THE PREVIOUS FRACTURE OR A NEW ONE FORMED AS A RESULT OF THE CERCLAGE WIRE FRACTURE. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2017 - 10871, 0001825034 - 2017 - 10874, 0001825034 - 2017 - 10873.

    Description of Event or Problem · 1

    IT WAS REPORTED FROM A CLINICAL STUDY THAT THE PATIENT WAS EXPERIENCING MODERATE LEFT HIP PAIN, DIFFICULTIES AMBULATING, DIFFICULTY PERFORMING ACTIVITIES OF DAILY LIVING AT A THREE YEAR FOLLOW UP AFTER PRIMARY SURGERY. NO OTHER ADDITIONAL INFORMATION WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    594570 REGENEREX ACETABULAR SHELL 64ODX54ID HIP PROSTHESIS LPH ZIMMER BIOMET, INC. N/A 478150

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Other