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

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    Filters FDA Recall × Status: Open, Classified × Clear all

    VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.

    FDA Recall
    Open, Classified ·LivaNova USA Inc·Product code LYJ·February 4, 2020

    Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053

    FDA Recall
    Open, Classified ·AtriCure, Inc.·Product code GEH·November 28, 2023

    Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056

    FDA Recall
    Open, Classified ·AtriCure, Inc.·Product code GEH·November 28, 2023

    VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

    FDA Recall
    Open, Classified ·LivaNova USA Inc·Product code LYJ·November 16, 2018

    DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

    DigitalDiagnost C90 High Performance, used to acquire, process, store, display and export digital radiographic images.

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

    MediBeads Neck Wrap, Item Number 34320

    FDA Recall
    Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

    ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code JAA·September 20, 2022

    CombiDiagnost R90 R.1.0

    FDA Recall
    Open, Classified ·Philips North America·Product code JAA·March 3, 2023

    PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.

    FDA Recall
    Open, Classified ·Preat Corp·Product code EMA·February 1, 2023

    CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

    CombiDiagnost R90; Model Number: 709031;

    FDA Recall
    Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025

    ProxiDiagnost N90. radiography and fluoroscopy system

    FDA Recall
    Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany·Product code JAA·May 19, 2021

    IonoStar Plus, Catalog (REF) Numbers: a) 2540, b)2543, c) 2544, d) 2545, e) 2546, f) 2547, g) 2549; dental cement

    FDA Recall
    Open, Classified ·Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany·Product code EMA·January 25, 2024

    Thermalon Eye Compress, Item Number 2434

    FDA Recall
    Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

    Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code JAA·June 10, 2022

    AXIOM Luminos Agile

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code JAA·December 9, 2022

    DigitalDiagnost C90 Release 3, used to acquire, process, store, display and export digital radiographic images.

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

    CombiDiagnost R90 Software Version R1.0 and R1.1

    FDA Recall
    Open, Classified ·Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany·Product code JAA·July 22, 2020

    CombiDiagnost R90 is multi-functional general R/F systems.

    FDA Recall
    Open, Classified ·Philips Healthcare·Product code JAA·September 22, 2021