BEUDAMED
    13 results · 12ms · Sources: EU EUDAMED, US FDA

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    Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.25GA Convenience Kit - XES VS0644.25-XES

    FDA Recall
    Open, Classified ·Vortex Surgical Inc.·Product code KDD·December 16, 2025

    FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic

    FDA Recall
    Open, Classified ·Inpeco S.A. Via San Gottardo 10 Lugano Switzerland·Product code CEM·September 3, 2025

    HENRY SCHEIN CRITERION EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)

    FDA Recall
    Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code FXX·December 21, 2023

    O&M Halyard SOFT TOUCH II Surgical Mask, Blue-Disposable surgical mask Product Code: 47500

    FDA Recall
    Open, Classified ·O & M HALYARD, INC.·Product code FXX·November 8, 2024

    O&M Halyard Procedure Mask with SO SOFT* Earloops, Yellow-Disposable surgical mask Product Code: 47117

    FDA Recall
    Open, Classified ·O & M HALYARD, INC.·Product code FXX·November 8, 2024

    PATTERSON PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)

    FDA Recall
    Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code FXX·December 21, 2023

    HENRY SCHEIN CRITERION ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)

    FDA Recall
    Open, Classified ·AMD Medicom Inc. 2555 Ch de L'Aviation Montreal Canada·Product code FXX·December 21, 2023

    FLUIDSHIELD 3 Fog-Free Procedure Mask with SO SOFT Lining and SO SOFT Earloops, Orange, WrapAround Visor Product Code 47147

    FDA Recall
    Open, Classified ·Owens & Minor Distribution, Inc.·Product code FXX·January 3, 2023

    (1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX; (3) GE Universal Viewer 8.0, Model 5865740-00x.

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code LLZ·July 15, 2022

    Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)

    FDA Recall
    Open, Classified ·Defibtech, LLC·Product code MKJ·October 14, 2024

    GE Healthcare Centricity Cardiology CA1000 (CA1000), Model Numbers: 1) 2033901-001; 2) 2038437-001; 3) 2038437-009; 4) 2038437-014; 5) 2038437-015 ; 6) 2038437-0XX; 7) 2109571-007; 8) 2109571-010; 9) 2109571-011; 10) 2109571-012; 11) MANLEGACY111; 12) MANLEGACY112; 13) MANLEGACY47; 14) P00011TS.

    FDA Recall
    Open, Classified ·GE Healthcare·Product code LLZ·February 19, 2025

    GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers: 1) 2022296-001; 2) 2033901-001; 3) 2038437-001; 4) 2038437-011; 5) 2038437-012; 6) 2038437-013; 7) 2038437-014; 8) 2038437-0XX; 9) 2098071-004; 10) 2109571-002; 11) 2109571-006; 12) 2109571-010; 13) 2109594-009; 14) 2109594-011; 15) K2090PS; 16) K2090PTED; 17) MANLEGACY114; 18) MANLEGACY64.

    FDA Recall
    Open, Classified ·GE Healthcare·Product code LLZ·February 19, 2025

    Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

    FDA Recall
    Open, Classified ·FX SHOULDER·Product code PHX·August 8, 2023