BEUDAMED
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    ACCU-CHEK COMFORT CURVE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·May 3, 2006

    DRILL SAW SPORTS 400

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·October 29, 2024

    SAW ATTACHMENT-SAGITTAL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·October 29, 2024

    COBAS 6000 CORE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·July 15, 2008

    LEG HOLDER, LOW PROFILE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code BWN·July 22, 2024

    BASEPLATE IMPACTOR, ASSEMBLY

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 1, 2024

    DRILL, 2.75MM, .066 CANNULATION

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·May 30, 2025

    DRILL, 2.75MM, .066 CANNULATION

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·May 30, 2025

    DRILL NON-CANNULATED, 4MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 30, 2025

    TIGHTROPE ® II RT WITH DEPLOYING SUTURE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·January 25, 2024

    SAW ATTACHMENT-SAGITTAL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·December 4, 2024

    DRILL NON-CANNULATED, 4MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·May 30, 2025

    SP FIBERTAK RC, DBLOAD TAPE BL/W, BLK/W

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·October 24, 2025

    BIO-COMP-TENOD SCRW W/DISP DRV 4.75X15MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWC·May 23, 2024

    COBAS C 303 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 27, 2024

    SUTR ANCH,BIO-COMP S-TAK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·December 20, 2024

    SUTR ANCH,BIO-COMP S-TAK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·December 20, 2024

    4-0 FIBERLOOP, 12 INCHES WITH NEEDLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GAT·October 25, 2023

    APOLLO RF® H50, ASPIRATING, ABLATOR, 50°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GEI·February 23, 2023

    BIO-COMP SWVLK C, CLD 4.75X19.1MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·December 16, 2024