BEUDAMED
    298 results · 23ms · Sources: EU EUDAMED, US FDA

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    EM2 NC AEM Monitor (NON-COM)

    FDA Recall
    Terminated ·Encision, Inc.·Product code GEI·June 23, 2003

    EM2M NC AEM Monitor, (NON-COM)

    FDA Recall
    Terminated ·Encision, Inc.·Product code GEI·June 23, 2003

    EM2+A NC AEM Monotor (NON-COM)

    FDA Recall
    Terminated ·Encision, Inc.·Product code GEI·June 23, 2003

    Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code MWS·October 16, 2024

    Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code MWS·October 16, 2024

    ACROBAT-i Vacuum Stabilizer System, Part Number C-OM-10000. Component of a chest stabilization system for cardiac and chest surgery.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DWS·June 28, 2023

    ACROBAT SUV Vacuum Off-Pump System, Part Number C-OM-9000S. Component of a chest stabilization system for cardiac and chest surgery.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DWS·June 28, 2023

    ACROBAT V Vacuum Off-Pump System, Part Number C-OM-9100S. Component of a chest stabilization system for cardiac and chest surgery.

    FDA Recall
    Open, Classified ·Maquet Cardiovascular, LLC·Product code DWS·June 28, 2023

    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

    FDA Recall
    Terminated ·CareFusion 303, Inc.·Product code FRN·July 21, 2015

    (1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802, Laser System; and (3) Lumenis Pulse 120H, REF GA-0008700, Laser System.

    FDA Recall
    Open, Classified ·LUMENIS, LTD. Yokneam Ind. Park 6, Ha-Kidma Yokne'Am Ilit Israel·Product code GEX·January 23, 2025

    Ulnar Shorting Saw Blade is labeled in part: "Congruent Bone Plates, SIZE Ulnar Shortening Saw Blade - Hub Style S, REF 80-0499-S, Material: Stainless Steel, STERILE, Rx Only, ACUMED, Hillsboro, OR, USA". The Ulnar Saw Blade is an accessory used with a Congruent Bone Plate System covered under K012655, but it is labeled and sold separately by itself. The saw blade is also sold as part of the Upper Extremity Osteotomy System (BOM 15-0030). The BOM 15-0030 system does not have a label, but the saw blade is individually labeled and shipped together with this system when it is ordered. Intended use: Cutting Bones

    FDA Recall
    Terminated ·Acumed LLC·Product code HRS·April 14, 2010

    Bari Maxx II, KCI''s BariMaxx II bariatric bed, P/N 310611, November 2001, KCI The Clinical Advantage, P. O. Box 659508, San Antonio, Texas 78265-9508, Call Toll Free 1-800-531-5346, FAX (210) 308-3998, Http://www.kci1.com

    FDA Recall
    Terminated ·Kinetic Concepts, Inc·Product code FNL·August 16, 2004

    Large Stealth Chamber, Catalog Numbers: DS50-001-XL-T, DS50-002-XL-T, DS50-003-XL-T, DS50-102-XL-T, DS50-103-XL-T

    FDA Recall
    Terminated ·Iba Dosimetry·Product code IYE·April 26, 2017

    Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28 P99-110-4630

    FDA Recall
    Terminated ·Paragon 28, Inc. 14445 Grasslands Dr Englewood CO 80112-7062·Product code HTW·July 30, 2021

    Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S

    FDA Recall
    Open, Classified ·Paragon 28, Inc. 14445 Grasslands Dr Englewood CO 80112-7062·Product code HSB·October 13, 2025

    Kit Model #650305414, MTO Left Heart with DT Boulder Com Hosp - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any combination of devices from the NAMIC Fluid Management finished good product families and potentially other devices designed and manufactured by original equipment manufacturers (OEM).

    FDA Recall
    Terminated ·Medline Industries Inc·Product code OEQ·September 14, 2020

    CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit

    FDA Recall
    Terminated ·Avanos Medical, Inc.·Product code PSG·March 16, 2020

    HammerTube Implant, 2.75mm, 10 Cannulated (Sterile)

    FDA Recall
    Open, Classified ·Paragon 28, Inc. 14445 Grasslands Dr Englewood CO 80112-7062·Product code HTY·May 26, 2022

    3M Steri-Drape, Large Towel Drape, REF 1010NS, general surgery drape

    FDA Recall
    Open, Classified ·3M Healthcare Business·Product code PUI·October 6, 2022

    3M Steri-Drape, Large Towel Drape, REF 1010NSD, general surgery drape

    FDA Recall
    Open, Classified ·3M Healthcare Business·Product code PUI·October 6, 2022