BEUDAMED
    96 results · 16ms · Sources: EU EUDAMED, US FDA

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    GlideScope Go Monitors

    FDA Recall
    Open, Classified ·Verathon, Inc.·Product code CCW·July 1, 2021

    Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider

    FDA Recall
    Open, Classified ·Turbett Surgical, Inc.·Product code FRG·December 5, 2022

    Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider

    FDA Recall
    Open, Classified ·Turbett Surgical, Inc.·Product code FRG·December 5, 2022

    Centricity Enterprise Web

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity Universal Viewer Zero Footprint Client

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity Radiology RA600

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity Cardiology CA1000

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Centricity PACS RA1000

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·April 28, 2022

    Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code CBK·June 14, 2021

    A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minimum Ventilatory Support, Facility Use

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code MNS·June 14, 2021

    A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code MNS·June 14, 2021

    Mito Red Light, Super Mobile

    FDA Recall
    Open, Classified ·MITO RED LIGHT INC·Product code ILY·February 12, 2025

    Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180

    FDA Recall
    Open, Classified ·Boston Scientific Neuromodulation Corporation·Product code LGW·April 29, 2026

    Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1

    FDA Recall
    Open, Classified ·Busse Hospital Disposables, Inc.·Product code OGJ·October 21, 2022

    Cirq Arm System 2.0

    FDA Recall
    Open, Classified ·Brainlab AG Olof-palme-str. 9 Munich Germany·Product code OLO·March 2, 2023

    Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1

    FDA Recall
    Open, Classified ·Busse Hospital Disposables, Inc.·Product code OGJ·October 21, 2022

    Brand Name: Paradise Ultrasound Renal Denervation System Product Name: Paradise Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation

    FDA Recall
    Open, Classified ·ReCor Medical Inc.·Product code QYI·January 29, 2026

    FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code QZI·June 25, 2025

    Brand Name: Paradise Ultrasound Renal Denervation System Product Name: Paradise Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation

    FDA Recall
    Open, Classified ·ReCor Medical Inc.·Product code QYI·January 29, 2026

    Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1

    FDA Recall
    Open, Classified ·Covidien·Product code GDY·February 21, 2024