BEUDAMED
    23 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

    Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1

    FDA Recall
    Open, Classified ·Skytron, Div. The KMW Group, Inc·Product code FQO·March 5, 2020

    Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32

    FDA Recall
    Open, Classified ·Skytron, Div. The KMW Group, Inc·Product code FQO·May 11, 2021

    Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A

    FDA Recall
    Open, Classified ·Skytron, Div. The KMW Group, Inc·Product code FQO·June 2, 2022

    MediBeads Neck Wrap, Item Number 34320

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

    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

    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

    Thermalon Neck Wrap, Item Number 24322

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

    Thermalon Stye Compress, Item Number 24352

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

    Thermalon Heating Pad, Item Number 24002

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

    DENTEMP ONE STEP .077OZ, SKU 902139

    FDA Recall
    Open, Classified ·Family Dollar Stores, Llc.·Product code EMA·October 4, 2023

    Ionolux, Catalog (REF) Numbers: a) 2115, b)2117, c) 2118, d) 2119, e) 2120, f) 2122; dental cement

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

    MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R

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

    Thermalon Sinus Compress, Item Number 24332

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

    Thermalon Back Wrap, Item Number 24312

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

    DENTEMP ONE STEP .077OZ, SKU 902139

    FDA Recall
    Open, Classified ·Family Dollar Stores, Llc.·Product code EMA·June 23, 2022