BEUDAMED
    28 results · 14ms · Sources: EU EUDAMED, US FDA

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    125 series iGO2 Portable Oxygen Concentrator-indicated for the administration of supplemental oxygen. Models: 125D, 125D-XB

    FDA Recall
    Open, Classified ·DeVilbiss Healthcare LLC·Product code CAW·September 19, 2022

    DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR, Model Numbers 1025DS, 1025UK, 1025KS, and 1025KS-AR

    FDA Recall
    Open, Classified ·DeVilbiss Healthcare LLC·Product code CAW·March 9, 2023

    JMC5A Ni/TruAire-5 Oxygen Concentrator, Model: O2C5L

    FDA Recall
    Open, Classified ·JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD No·Product code CAW·December 9, 2024

    DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q

    FDA Recall
    Open, Classified ·DeVilbiss Healthcare LLC·Product code CAW·November 18, 2022

    iGo2 DC Car Adapter to be used with iGo2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.

    FDA Recall
    Open, Classified ·Medical Depot Inc.·Product code CAW·April 11, 2025

    GCE HEALTHCARE Zen-O lite, Portable Oxygen Concentrator, Model RS-00608-X-S

    FDA Recall
    Open, Classified ·Ohio Medical Corporation·Product code CAW·May 8, 2025

    Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)

    FDA Recall
    Open, Classified ·Invacare Corporation·Product code CAW·June 10, 2022

    SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600

    FDA Recall
    Open, Classified ·Philips Respironics, Inc.·Product code CAW·October 7, 2025

    React Health PHOENIX 5L Oxygen Concentrator

    FDA Recall
    Open, Classified ·3B Medical, Inc. 5475 Rings Rd Ste 550 Dublin OH 43017-7537·Product code CAW·February 4, 2026

    LOM Disposable Surgical Gowns/Medical Gowns, Single-Use

    FDA Recall
    Open, Classified ·THREAD COUNSEL INC DBA LAWS OF MOTION·Product code FYA·September 17, 2020

    NavitrackER Kit A: Knee, Model Number 20-8000-000-07,

    FDA Recall
    Open, Classified ·Orthosoft, Inc. dba Zimmer CAS 3300-75 Queen St Montreal Canada·Product code OLO·January 7, 2022

    biokitHSV-2 Rapid Test, REF: 300028001

    FDA Recall
    Open, Classified ·Biokit, S.A. Avinguda De Can Montcau 7 (Barcelona) Llica D'Amunt Spain·Product code LGC·September 28, 2022

    Ocean Water Seal Chest Drains (Ocean): Products REF Number Product Name (1)2002-000 DRAIN, OCEAN SINGLE W/AC,S; (2)2002-040 DRAIN, OCEAN SINGLE,PEDI CONNECTOR; (3)2002-100 DRAIN, OCEAN SINGLE W/AC; (4)2002-300 DRAIN, OCEAN SINGLE W/S; (5) 2002-400 DRAIN, OCEAN SINGLE ; (6)2012-320 DRAIN, OCEAN PEDI W/S; (7)2050-000 DRAIN, OCEAN BRU W/AC,S

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code CAC·September 18, 2023

    SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Anticoagulation assemblies are indicated for use with an autotransfusion system between the suction tip and reservoir.

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code CAC·November 27, 2018

    Atrium Oasis Drain Single W / AC, Part No. 3600-100

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code CAC·November 1, 2023

    Atrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3650-100, DRAIN, OASIS BRU W/AC, 3650 ATS BLOOD RECOVERY

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code CAC·September 5, 2023

    Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code CAC·December 13, 2023

    Tec 850 ISO Anesthesia Vaporizer, Reference Number 1177-9850-ISO

    FDA Recall
    Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

    Tec 6 Plus Anesthesia Vaporizer, Reference Numbers 1107-9601-000, 1107-9602-000, 1107-9603-000, 1107-9604-000, 1107-9610-000, 1107-9612-000, 1107-9616-000, 1107-9617-000, 2066835-001, 2069767-001, 2078800-001, 2091008-001, 2091009-001, M1098876, M1145610, M1220023, M1220854, M1221495, and M1233992

    FDA Recall
    Open, Classified ·GE Medical Systems, LLC·Product code CAD·November 18, 2024

    Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.

    FDA Recall
    Open, Classified ·Draeger, Inc.·Product code CAD·November 24, 2025