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

    FULL VISION INC. TRACKMASTER,TREADMILL TMX428 220V, Model #317-07927

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE CHINA

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    Actim PROM dipstik, REF 30831ETUS; qualitative immunoassay rapid test for rupture of fetal membrane

    FDA Recall
    Open, Classified ·ACTIM OY Klovinpellontie 3 Espoo Finland·Product code OAM·November 23, 2023

    Proteus 235- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation

    FDA Recall
    Open, Classified ·Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium·Product code LHN·June 14, 2021

    Proteus 235-Proton Therapy System

    FDA Recall
    Open, Classified ·Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium·Product code LHN·May 26, 2021

    Proteus235- Proton Therapy System: to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation

    FDA Recall
    Open, Classified ·Ion Beam Applications S.A. 3 Chemin Du Cyclotron Louvain-la-neuve Belgium·Product code LHN·April 20, 2022

    ProteusPLUS and ProteusONE- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation Proteus 235

    FDA Recall
    Open, Classified ·Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium·Product code LHN·February 15, 2022

    Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection images for the reconstruction of a 3D view. The device is operated and used by qualified healthcare professionals.

    FDA Recall
    Open, Classified ·Palodex Group Oy Nahkelantie 160 Tuusula Finland·Product code OAS·October 28, 2021