BEUDAMED
    50 results · 62ms · Sources: EU EUDAMED, US FDA

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    XEN 45 GTS

    FDA Adverse Event
    Injury ·ALLERGAN (IRVINE)·Product code KYF·December 6, 2023

    UNKNOWN LOCKING PLATE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRS·August 17, 2017

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·July 24, 2012

    UNKNOWN LOCKING PLATE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRS·August 17, 2017

    PARADIGM INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·January 30, 2019

    PRGDM INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 30, 2019

    620G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 30, 2019

    VERSACARE MED SURG BED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FNL·May 29, 2026

    VERSACARE MED SURG BED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FNL·February 24, 2026

    VERSACARE MED SURG BED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FNL·February 10, 2025

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code LWR·May 16, 2018

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·March 4, 2025

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·April 20, 2026

    TORQUE LIMITING DRIVER HANDLE

    FDA Adverse Event
    Injury ·TECOMET, INC.·Product code LXH·November 17, 2023

    HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·June 27, 2022

    HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·June 27, 2022

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 10, 2012

    "***REF IWTH56***Certain EP HEALING ABUTMENT 5mm(D) X 5mm(P) X 6mm(H).*** Healing abutment*** STERILE.***Rx Only.*** Made in USA*** Implant Innovations, Inc. Global Headquarters 4555 Riverside Drive, Palm Beach Gardens, FL 33410 USA Tel: (800) 342-5454 www.3i.online.com. Outside US 561-776-6700***Implant Innovations Siberica S.L., WTC Almeda Park, Ed. 1 Planta 1a Pl. De la Pau s/n 08940-Cornella de Llobregat (Barcelona) Spain. Phone: +34 934 705500. Fax +34 933 717 849. Lot Number: 602691.***" Biomet 3i healing abutments are temporary healing abutments for use in maintaining the soft tissue opening throughout the healing process of dental restoration.

    FDA Recall
    Terminated ·Biomet 3i, LLC·Product code NSQ·February 23, 2010

    GORE® TAG® CONFORMABLE THORACIC STENT GRAFT WITH ACTIVE CONTROL SYSTEM

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·April 17, 2025

    TIBIAL COMP,SINGLECOATED US VERSION, LARGE

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code NTG·December 17, 2015