BEUDAMED
    FDA Adverse Event Injury Summary report: N

    POROUS FINN STEM 89MMX15.5

    MDR report key: 9345438 · Received November 19, 2019

    Report

    Report Number
    0001825034-2019-05284
    Event Type
    Injury
    Date Received
    November 19, 2019
    Report Date
    November 19, 2019
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JWH
    PMA / PMN Number
    N/A
    Removal / Correction Number
    N/A
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). CONCOMITANT MEDICAL PRODUCTS: THERAPY DATE: UNKNOWN. BIOMET INTERLOK STEM TIBIAL COMPONENT, CATALOG # 141513, LOT # 357860. VANGUARD PS TIBIAL BEARING, CATALOG # 185092, LOT # 192510. VANGUARD INTERLOK FEMORAL COMPONENT, CATALOG # 183326, LOT # 156230. BIOMET POROUS FINN STEM, CATALOG # CP163826, LOT # 784950. VANGUARD POST FEMORAL AUGMENT, CATALOG # 184226, LOT # 861350. BIOMET TIBIAL BLOCK, CATALOG # 141763, LOT # 959760. VANGUARD AUGMENT BOLT, CATALOG # 184299, LOT # 861460. VANGUARD POST FEMORAL AUGMENT, CATALOG # 184246, LOT # 258970. VANGUARD DISTAL FEMORAL AUGMENT, CATALOG # 184266, LOT # 677130 VANGUARD DISTAL FEMORAL AUGMENT, CATALOG # 184286, LOT # 677160. NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. THE DHR WAS REVIEWED AND NO DISCREPANCIES RELEVANT TO THE REPORTED EVENT WERE FOUND. MEDICAL RECORDS WERE NOT PROVIDED. THE ROOT CAUSE OF THE REPORTED ISSUE IS ATTRIBUTED TO PATIENT CONDITION. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2019-00002, 0001825034-2019-00005, 0001825034-2019-00006, 0001825034-2019-05275, 0001825034-2019-05278, 0001825034-2019-05279, 0001825034-2019-05280, 0001825034-2019-05281, 0001825034-2019-05282, 0001825034-2019-05283.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT HAS DEVELOPED AN ALLERGY. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1137463 POROUS FINN STEM 89MMX15.5 PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 799930

    Patients

    Seq Age Sex Outcome Treatment
    1 Other