BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    ARCOS 22X150MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018

    TAPERLOC STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018

    G7 PPS LTD ACETABULAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·October 11, 2018

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FSA·January 17, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014

    CAPSURE SP NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    TAPERLOC STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 26, 2023

    CER OPTION TYPE 1 TAPER SLEVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 6, 2018

    CER BIOLOXD OPTION HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·August 7, 2018

    AS LVP 20D DEHP 2SS CV

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·July 24, 2020