BEUDAMED
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    SCREWCOG

    FDA UDI
    MEDYGLOBAL MEDICAL DEVICES SL.·B772DWB2101·PDO THREADS BIOABSORBABLE MATERIAL WITH NEEDLE

    SP 2.6 MM KNOTLESS FIBERTAK ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·February 27, 2024

    AEQUALIS REVERSED GLENOID SPHERE

    FDA Adverse Event
    Injury ·Product code KWS·January 21, 2020

    AEQUALIS REVERSED INSERT

    FDA Adverse Event
    Injury ·Product code KWS·January 21, 2020

    UNIVERSAL GLENOID INLAY SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·February 26, 2024

    AEQUALIS REVERSED INSERT

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·February 28, 2019

    TORNIER

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code KWS·March 19, 2010

    BIO-COMP SWVLK SP, 4.75X24.5MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·June 21, 2024

    FIBERTAPE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·June 21, 2024

    ACL TIGHTROPE RT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MBI·February 18, 2025

    S5 ROLLER PUMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWB·April 13, 2021

    10.0 MM FLIP CUTTER II

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HWE·August 12, 2024

    DW ARTHROSCOPY FLUID MANAGEMENT DEV

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRX·December 29, 2023

    BURR, STRAIGHT, 13MM DIAM. 2.0 MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 14, 2024

    FIBERTAK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·December 28, 2023

    Ø8X 20MM BC IF SCRW, VENTED

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MAI·December 17, 2025

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MBI·March 1, 2024

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·May 27, 2025

    GLENOID, PE WITH PEG, SMALL

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KWS·August 7, 2024

    Sarns 8000 Cardioplegia Monitor, Catalog Number 16414; also known as PROG COMP BD AMPRO 420 CPG 8K, Catalog Number 816373 The Sarns 8000 Cardioplegia Monitor is indicated to measure extracorporeal line pressure and signal when the pressure exceeds the operator-set limit.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corporation·Product code DWB·August 29, 2011