BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HFN A/R SCREW 80MM

    MDR report key: 19070937 · Received April 9, 2024

    Report

    Report Number
    0001825034-2024-00972
    Event Type
    Injury
    Date Received
    April 9, 2024
    Report Date
    August 6, 2024
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    HSB
    UDI-DI
    00887868038716
    PMA / PMN Number
    K100238
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PL
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY CORRECTED INFORMATION. THE FOLLOWING SECTIONS WERE UPDATED: B4; B5; D2; G2; G3; G6; H1; H2 UPON RECEIVING ADDITIONAL INFORMATION OF THE REPORTED EVENT, IT WAS DETERMINED THAT THE PRODUCT WAS NOT INVOLVED IN THE EVENT. THE INITIAL REPORT SHOULD BE VOIDED. 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.

    Additional Manufacturer Narrative · 0

    (B)(4). D10: MEDICAL PRODUCTS: ITEM#: 814510110, HFN LAG SCREW 10.5MM X 110MM; LOT#: TC1132310A; ITEM#: 814503000, HFN END CAP FLUSH; LOT#: TD1113 B; ITEM#: 814511180, HFN 130 DEG 11MM X 180MM; LOT#: 748660. G2: FOREIGN: POLAND. H3: CUSTOMER HAS INDICATED THAT THE PRODUCT IS IN PROCESS OF BEING RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.

    Description of Event or Problem · 0

    NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP FRACTURE SURGERY APPROXIMATELY SEVEN (7) YEARS AGO, SUBSEQUENTLY, THE PATIENT IS ABLE TO PALPATE THE LAG SCREW THROUGH THE SKIN AND WAS CAUSING THE PATIENT DISCOMFORT. THE PATIENT UNDERWENT A REVISION SURGERY ON AND UNKNOWN DATE AND ALL IMPLANTS WERE REMOVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    456482 HFN A/R SCREW 80MM ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES HSB ZIMMER BIOMET, INC. SP1122280F 00887868038716

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention| H