BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HYPE SCL 7 LATERALIZED CEMENTLESS STEM

    MDR report key: 21136464 · Received January 13, 2025

    Report

    Report Number
    3008668801-2025-00012
    Event Type
    Injury
    Date Received
    January 13, 2025
    Date of Event
    December 17, 2024
    Report Date
    February 9, 2026
    Manufacturer
    S.E.R.F SOCIETE DETUDES RECHERCHE FABRICATION
    Product Code
    LZO
    PMA / PMN Number
    K223745
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    AN EVALUATION OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE WAS NOT RETURNED TO THE MANUFACTURER. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE IT WILL BE REPORTED IN A SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION.

    Additional Manufacturer Narrative · 0

    MANUFACTURER ENTITY D3 CORRECTED TO S.E.R.F SOCIETE DETUDES RECHERCHE FABRICATION.

    Additional Manufacturer Narrative · 0

    ADDITION OF LOT CODE IN SECTION D4. CORRECTION OF PRODUCT CODE IN SECTION D2B. CORRECTION OF PRODUCT DEVICE NAME IN SECTION D2A. INVESTIGATION CONCLUSION: REPORTED EVENT: AN EVENT REGARDING INSTABILITY (LEADING TO REVISION) INVOLVING AN HYPE SCL 7 LATERALIZED CEMENTLESS STEM WAS REPORTED. THE REPORTED DEVICE IS AN SERF PRODUCT. DOCUMENTARY INVESTIGATION: NO NON-CONFORMITIES OBSERVED ON THIS BATCH 16 UNITS PLACED ON THE MARKET BY SERF IN (B)(6) 2012 NO OTHER COMPLAINTS HAVE BEEN REGISTERED FOR THIS BATCH ABSENCE OF TECHNICAL INVESTIGATION: NO PRODUCT RETURN - COMPLAINT RELATED TO A CLINICAL STUDY IN THE ABSENCE OF FURTHER INFORMATION, THE CAUSE CANNOT BE DETERMINED.

    Description of Event or Problem · 0

    SERF REPORTED RECEIVING RESULTS OF A CLINICAL STUDY. REVISION FOR INSTABILITY.

    Description of Event or Problem · 0

    SERF REPORTED RECEIVING RESULTS OF A CLINICAL STUDY. REVISION FOR INSTABILITY.

    Description of Event or Problem · 0

    SERF REPORTED RECEIVING RESULTS OF A CLINICAL STUDY. REVISION FOR INSTABILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    499507 HYPE SCL 7 LATERALIZED CEMENTLESS STEM PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CEMENTLESS LZO S.E.R.F SOCIETE DETUDES RECHERCHE FABRICATION 1107179A

    Patients

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