BEUDAMED
    59 results · 27ms · Sources: EU EUDAMED, US FDA

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    American Surgical Cylindrical Sponges-Strung 1/2" x 1.5" Ref Number: 70-02 Product Usage: Neurosurgical and Nonneurosurgical Sponges

    FDA Recall
    Terminated ·American Surgical Company·Product code EFN·March 31, 2016

    FABCO ORS DENTAL ROLLS, 1-1/2" STERILE, COTTON 3/8" Diameter x 1-1/2" (9.5mm x 38.1mm), packaged 5 /Pouch, 50 Pouches/Box Reorder Number: 34911510

    FDA Recall
    Open, Classified ·Carwild Corporation·Product code EFN·August 2, 2022

    Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm x 75cm (CFN CH05-40-75US), 6mm x 40mm x 75cm (CFN CH06-40-75US), 7mm x 40mm x 75cm (CFN CH07-40-75US), 8mm x 40mm x 75cm (CFN CH08-40-75US), 9mm x 40mm x 75cm (CFN CH09-40-75US), 10mm x 40mm x 75cm (CFN CH10-40-75US), 12mm x 40mm x 75cm (CFN CH12-40-75US)

    FDA Recall
    Open, Classified ·Product code LIT·September 19, 2024

    Oxford/Oxbridge AFN End Cap 10 mm x 5 mm tp 12 mm x10 mm The end caps are a circular disk with a small threaded shaft to be screwed to the distal end of the Nail.

    FDA Recall
    Terminated ·Ortho Solutions Inc·Product code HSB·April 19, 2017

    TourniKwik Tourniquet Set (CFN 79012)

    FDA Recall
    Open, Classified ·Medtronic Perfusion Systems·Product code GDJ·May 16, 2024

    Enhanced Verify Evaluation Handset (CFN HH90130FA)

    FDA Recall
    Open, Classified ·Medtronic Neuromodulation·Product code EZW·April 3, 2025

    Puritan Bennett 560 Ventilator, PB560, CFN 4096600

    FDA Recall
    Open, Classified ·Covidien Llc·Product code QOS·August 19, 2022

    InPen App, Model/CFN Number: MMT-8061 (Android Users)

    FDA Recall
    Open, Classified ·Medtronic MiniMed, Inc.·Product code NDC·November 13, 2025

    O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000

    FDA Recall
    Terminated ·Medtronic Navigation, Inc.-Littleton·Product code OWB·November 15, 2019

    Covidien Emprint Ablation Catheter with Thermosphere Technology Bronchoscopic Ablation, CFN CA108L1

    FDA Recall
    Terminated ·Covidien Llc·Product code NEY·September 29, 2021

    TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter

    FDA Recall
    Open, Classified ·GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland·Product code DPZ·May 19, 2023

    InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users)

    FDA Recall
    Open, Classified ·Medtronic MiniMed, Inc.·Product code NDC·June 16, 2025

    Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72

    FDA Recall
    Completed ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVY·November 8, 2021

    Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); CFN: SIGSDL45CTVT;

    FDA Recall
    Open, Classified ·Product code GDW·September 25, 2025

    A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).

    FDA Recall
    Open, Classified ·Medtronic Neuromodulation·Product code LGW·December 3, 2025

    Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;

    FDA Recall
    Open, Classified ·Product code GDW·September 25, 2025

    Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & accessories22 Product Number/CFN: 178083, 178093, 178094

    FDA Recall
    Open, Classified ·Product code GEI·March 5, 2021

    Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems. Product Number/CFN: 186-0208 UDI-Device Identifier (GTIN/UPN): 10884521130319

    FDA Recall
    Open, Classified ·Covidien LLC·Product code OLW·July 26, 2018

    SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D

    FDA Recall
    Open, Classified ·Medtronic Neuromodulation·Product code LKK·November 21, 2024

    SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C

    FDA Recall
    Open, Classified ·Medtronic Neuromodulation·Product code LKK·November 21, 2024