BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BIOMET ARCOM AP PAT 3PST 31MM SM

    MDR report key: 25243484 · Received May 21, 2026

    Report

    Report Number
    0001825034-2026-01433
    Event Type
    Injury
    Date Received
    May 21, 2026
    Report Date
    May 19, 2026
    Manufacturer
    ZIMMER BIOMET, INC.
    Product Code
    JWH
    PMA / PMN Number
    NI
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4). D10: 11-146554, MAXIM PS TIBIAL BEARING, LOT: 706330 . 145132, MAXIM PS FEMORAL COMPONENT , 365040. 141314, MAXIM MODULAR FINNED STEM, LOT: 765220. 141213, MAXIM PRIMARY TIBIAL PLATE, 002650 . UNKNOWN, PALACOS CEMENT, UNK LOT. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE 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

    IT WAS REPORTED THAT THE PATIENT UNDERWENT A LEFT PRIMARY TOTAL KNEE ARTHROPLASTY ABOUT 26 YEARS AGO, SUBSEQUENTLY APPROXIMATELY 6 TO 8 WEEKS POST-IMPLANTATION REQUIRED MANIPULATION UNDER ANESTHESIA BECAUSE THE KNEE ¿FROZE UP.¿ NO ADDITIONAL SURGICAL OR MEDICAL INTERVENTIONS WERE REPORTED TO DATE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    214364 BIOMET ARCOM AP PAT 3PST 31MM SM PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 571730

    Patients

    Seq Age Sex Outcome Treatment
    1