BEUDAMED
    30 results · 18ms · 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

    Cardiovascular Custom Procedure Kits, REV :10. REV 13, REV17, REV 18 FX X-Coated Perfusion Pack Item Number: 72941 Terumo Cardiovascular Systems, Ashland, MA 01721 The Cardiovascular Procedure Kits are indicated for use only in the extracorporeal circuit for the cardiopulmonary bypass procedure(s) for which the user designed it. The 3-T L. V. Control Valve is a one-way vent valve used during cardiopulmonary bypass surgery to help prevent the buildup of excess vacuum pressure when suctioning either from the heart or the surgical field, and to help prevent inadvertent retrograde now and air into the heart.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code MJJ·August 11, 2011

    Ear Loop Procedure Masks, For one time use only, Glass-Free, Reorder No. 2201, packed in a cardboard box (unit box). Manufactured for dynarex Corporation, Brewster, NY 10509. Made in China. Product is labeled with a Latex-free symbol that states ''This product does not contain any natural rubber latex'' . A total of 50 masks are in one unit box, and 12 boxes are placed into one shipping carton/case.

    FDA Recall
    Terminated ·Dynarex Corporation·Product code FXX·December 31, 2002

    Ear Loop Procedure Masks With Plastic Shield, For one time use only, Glass-Free, Reorder No. 2202, packed in a cardboard box (unit box). Manufactured for dynarex Corporation, Orangeburg, NY 10962. Made in China. Product is labeled with a Latex-free symbol that states ''This product does not contain any natural rubber latex'' . A total of 50 masks are in one unit box, and 4 boxes are placed into one shipping carton/case.

    FDA Recall
    Terminated ·Dynarex Corporation·Product code FXX·December 31, 2002

    MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040

    FDA Recall
    Terminated ·AMD Medicom Inc.·Product code FXX·October 11, 2019

    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

    Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is manufactured and distributed by Maytex Corporation, CA Ear-loop face mask for basic medical/dental procedures.

    FDA Recall
    Terminated ·Maytex Corp·Product code FXX·May 15, 2013

    Supergrade Earloop Masks, surgical mask; 50 masks per box; Distributed by Safco Dental Supply Co., Northbrook, IL 60062

    FDA Recall
    Terminated ·Safco Dental Supply Co. Inc.·Product code FXX·June 3, 2003

    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

    MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 3 MASKS, Item Code 2042

    FDA Recall
    Terminated ·AMD Medicom Inc.·Product code FXX·October 11, 2019

    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

    Centricity Universal Viewer 7.0, Model 5829628-0XX. Radiological image processing system

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code LLZ·August 12, 2021

    (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

    GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d) 2052782-00x

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code LLZ·May 22, 2019

    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