BEUDAMED
    26 results · 20ms · 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 ×

    Calculator/ Data Processing Module for Clinical Use

    FDA Recall
    Terminated ·Misys Healthcare Systems·Product code JQP·July 24, 2003

    Custom Angiographic Kit

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code DQO·February 13, 2003

    Custom Angiographic Kit.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code DQO·February 13, 2003

    Custom Angiographic Kit

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code DQO·February 13, 2003

    Cidex Plus Test Strips

    FDA Recall
    Terminated ·Advanced Sterilization Products·Product code JOJ·December 17, 2003

    Uroview 2600 Uroview System

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·May 12, 2003

    Multi Absorbers, reference number 8003138

    FDA Recall
    Terminated ·Datex-Ohmeda·Product code BSF·February 12, 2003

    Uroview 2000 X-ray System

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·May 12, 2003

    Uroview 2500 X-ray System

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·May 12, 2003

    OmniDiagnost System

    FDA Recall
    Terminated ·Philips Medical Systems Sales & Service Region No. America·July 17, 2003

    Diagnost 97

    FDA Recall
    Terminated ·Philips Medical Systems Sales & Service Region No. America·July 17, 2003

    Synapse Version 2.2.1 and 2.3.1 software

    FDA Recall
    Terminated ·Fujifilm Medical System USA, Inc.·Product code LLZ·May 12, 2003

    Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Diagnostic, manufactured by Zeus Scientific, Inc., Raritan, NJ.

    FDA Recall
    Terminated ·Zeus Scientific Inc·Product code LFZ·June 12, 2003

    CryoValve, Pulmonary Valve & Conduit

    FDA Recall
    Terminated ·Cryolife Inc·Product code NJK·September 10, 2003

    CryoValve, Aortic & Conduit

    FDA Recall
    Terminated ·Cryolife Inc·Product code MIE·September 10, 2003

    Multi Absorbers, reference number 8003138, in S/5 Aespire Start-up Kits (each containing 2 Multi Absorbers)

    FDA Recall
    Terminated ·Datex-Ohmeda·Product code BSF·February 12, 2003

    PER-FIT Percutaneous Dilational Tracheostomy Kit with Specialty Tracheostomy Tube REF # 511080

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JOH·December 12, 2003

    Modular Replacement System with Extra-Cortical Porous Coating, Femoral Module Stem and Tibial Module Stem

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics·Product code JDI·January 7, 2003

    Clinitek 50 Urine Chemistry Analyzer; Product codes 6509C, 6513K, 6514C, 6515C, 6516F and 6518C. [The different product codes are for the various countries where the product is distributed).

    FDA Recall
    Terminated ·Bayer Healthcare LLC 1884 Miles Ave Buildings 110 (Adlake), 17 & 18 Elkhart IN 46514-2291·Product code KQO·March 12, 2004

    Roche/Hitachi Modular Analytics P clinical chemistry analyzer; Modular P. Catalog number 766-8156.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·May 8, 2003