BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PLATE, FIXATION, BONE

    MDR report key: 7670039 · Received July 9, 2018

    Report

    Report Number
    8030965-2018-54859
    Event Type
    Injury
    Date Received
    July 9, 2018
    Date of Event
    March 12, 2018
    Report Date
    June 12, 2018
    Manufacturer
    OBERDORF SYNTHES PRODUKTIONS GMBH
    Product Code
    HRS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SN
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    PATIENT ID/INITIALS AND WEIGHT ARE UNKNOWN. DATE OF EVENT IS UNKNOWN; MARCH 12, 2018 IS THE DATE THE LITERATURE ARTICLE WAS PUBLISHED. THIS REPORT IS FOR AN UNKNOWN SYNTHES DYNAMIC HIP SYSTEM (DHS)/UNKNOWN LOT. PART AND LOT NUMBER ARE UNKNOWN; UDI NUMBER IS UNKNOWN. COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. (B)(4).

    Description of Event or Problem · 1

    THIS REPORT IS BEING FILED AFTER THE REVIEW OF THE FOLLOWING JOURNAL ARTICLE: CHAN L. ET AL (2018) NON-PROSTHETIC PERI-IMPLANT FRACTURES: CLASSIFICATION, MANAGEMENT AND OUTCOMES. ARCHIVES OF ORTHOPAEDIC AND TRAUMA SURGERY VOLUME 138, PAGES 791-802 ((B)(6)). THE AIMS OF THIS RETROSPECTIVE STUDY WERE TO REVIEW PATTERNS OF INJURY, MANAGEMENT AND OUTCOMES AND TO ATTEMPT TO CLASSIFY NON-PROSTHETIC PERI-IMPLANT FRACTURE (NPPIFS) INTO A SYSTEM THAT MAY AID FURTHER RESEARCH AND STUDY. A NON-PROSTHETIC PERI-IMPLANT FRACTURE (NPPIF) IS DEFINED AS A FRACTURE IN A BONE WITH AN EXISTING NON-PROSTHETIC IMPLANT SUCH AS AN EXTRAMEDULLARY PLATE AND SCREWS OR AN INTRAMEDULLARY NAIL. A TOTAL OF 53 PATIENTS 31 MALES AND 22 FEMALES WITH A MEAN AGE OF 64 YEARS (60 TOTAL NPPIFS) WERE INCLUDED IN THIS STUDY. OF THE 53 PATIENTS, 27 PATIENTS WERE REVISED WITH UNKNOWN SYNTHES DEVICES. AVERAGE FOLLOW-UP WAS 16 MONTHS (RANGE 0¿75). THE FOLLOWING POST-OPERATIVE COMPLICATIONS WERE OBSERVED. AN (B)(6) FEMALE PATIENT, INITIALLY IMPLANTED WITH AN UNKNOWN SYNTHES DHS OBTAINED NPPIF (INTERTROCHANTERIC) FRACTURE DUE TO A LOW VELOCITY FALL. PATIENT WAS REVISED WITH AN UNKNOWN SYNTHES ANTEGRADE FEMORAL NAIL, NO COMPLICATIONS WERE REPORTED AFTER REVISION SURGERY. THIS REPORT IS FOR AN UNKNOWN SYNTHES DYNAMIC HIP SYSTEM (DHS). THIS REPORT IS 5 OF 8 FOR (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    513663 PLATE, FIXATION, BONE HRS OBERDORF SYNTHES PRODUKTIONS GMBH

    Patients

    Seq Age Sex Outcome Treatment
    1 88 YR Required Intervention