BEUDAMED
    43 results · 12ms · 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 Recall × Status: Open, Classified × Clear all

    Temporary Titanium Abutments

    FDA Recall
    Open, Classified ·DDS Lab·Product code NHA·December 6, 2024

    Mega-Gen His Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80708-3; Mega-Gen Hers Personal Lubricant, 8 fl. oz., Meta Labs, UPC Code 80808-0 Product Usage: A topical gel that increases sexual excitement and pleasure.

    FDA Recall
    Open, Classified ·Altasource LLC dba Meta Labs LLC·Product code NA·February 3, 2014

    Nice-En-Smooth Berry Burst, 4 oz., Manufactured by Meta Labs LLC, UPC 80604-8 Product Usage: Flavored lubricant water based, condom friendly jelly used to enhance or replace a womans natural lubrication.

    FDA Recall
    Open, Classified ·Altasource LLC dba Meta Labs LLC·Product code NA·February 3, 2014

    Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The product is a nonprescription, topical gel that is used to enhance libido and stimulate orgasmic pleasure.

    FDA Recall
    Open, Classified ·Altasource LLC dba Meta Labs LLC·Product code NA·February 3, 2014

    Hot Ice, 1 fl. oz., Meta Labs LLC, UPC 80705-2 Product Usage: A topical gel that increases men and womens secual excitement and pleasure.

    FDA Recall
    Open, Classified ·Altasource LLC dba Meta Labs LLC·Product code NA·February 3, 2014

    BD Kiestra" ReadA; Catalog No.: 446948.

    FDA Recall
    Open, Classified ·BD KIESTRA LAB AUTOMATION Marconilaan 6 Drachten Netherlands·Product code JTQ·February 6, 2026

    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

    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

    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

    Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the battery that powers the AR-400 DrillSaw Sports 400 device.

    FDA Recall
    Open, Classified ·Arthrex, Inc.·Product code HAB·August 27, 2018

    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

    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

    ProxiDiagnost N90 R.1.0

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