BEUDAMED
    191 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall ×

    Medtronic AVE Everest PTCA Inflation Catheter 20 cc Item #AC2200

    FDA Recall
    Terminated ·Medtronic, Inc.·Product code LOX·January 31, 2003

    AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also as aid to search for individual positions providing relief in all delivery stages including postpartum period. Birthing bed is not intended for use as a general hospital bed.

    FDA Recall
    Open, Classified ·Linet Americas·Product code HDD·March 6, 2020

    EVEXIA LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF(s): EVE-11/EVE-X11, Rx Only, Not Sterile

    FDA Recall
    Open, Classified ·Ortho8, Inc.·Product code JOW·July 9, 2021

    Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended for use in operating theaters and intensive care

    FDA Recall
    Terminated ·Draeger Medical, Inc.·Product code FQO·September 30, 2013

    AVE 2 Birthing Bed

    FDA Recall
    Terminated ·Linet Spol. S.r.o. Zelevcice 5 Slany Czech Republic·Product code HDD·January 7, 2019

    Fujinon Endoscope Insertion Tube included with lower gastrointestinal EVE and lower gastrointestinal electronic video endoscopes.

    FDA Recall
    Terminated ·Fujinon Inc·Product code FDF·March 27, 2006

    Brand Name: Canturio Smart Extension Product Name: CSE Implant Model/Catalog Number: 43-5570-030-14 Product Description: Tibial stem extension for use with Zimmer Persona Personalized Knee System; 14mm diameter x 30mm height. Implantable device with integrated electronics for passive kinematic data collection. Single-use, sterile. Packaged in a sterile blister and outer shelf pack. Sold individually. Component: Yes. The Canturio Smart Extension (CSE) is a tibial implant component intended for use with the Zimmer Persona Personalized Knee System.

    FDA Recall
    Open, Classified ·Canary Medical, Inc.·Product code QPP·May 2, 2025

    ArthroCare brand OPUS Smartstitch Suture Cartridge, Catalog Number: OM-8071; Product is distributed by ArthroCare Corporation, 680 Vaqueros Ave., Sunnyvale, CA 94085

    FDA Recall
    Terminated ·ArthroCare Corporation·Product code KOG·June 7, 2006

    ArthroCare brand OPUS Smartstitch Magnum Wire Suture Cartridge, Catalog Number: OM-8075; Product is distributed by ArthroCare Corporation, 680 Vaqueros Ave., Sunnyvale, CA 94085

    FDA Recall
    Terminated ·ArthroCare Corporation·Product code KOG·June 7, 2006

    JOGRAPHY Cardiovascular Angiographic Catheter, 5F *** pigtail *** tapered with perfusion ports *** MEDI-DYNE, INC., 604 Queensbury Ave., Queensbury, New York 12804 *** Single use, sterile, disposable intravascular catheters with an atraumatic tip.

    FDA Recall
    Terminated ·Jomed Catheters, Inc.·November 21, 2002

    Shelhigh No-React Pulmonic Valve Conduit. **'Shelhigh No-React, Pulmonic Valve Conduit, NR4000-PA-C'** **'Shelhigh, Inc., 650 Liberty Ave., Union, NJ 07083 USA'** **'Shelhigh Porcine Pulmonic Valve Conduit Prosthesis Model NR-4000 Series with 'No-React' treatment*, INSTRUCTIONS FOR USE'**.

    FDA Recall
    Terminated ·Shelhigh, Inc.·Product code MWH·January 18, 2006

    Z2 Guiding Catheter 6 F JL3.5 SH Item No. : Z26JL35SH

    FDA Recall
    Terminated ·Medtronic, Inc.·March 17, 2003

    Z2 Guiding Catheter 6 F JR3.5 SH Item No. : Z26JR35SH

    FDA Recall
    Terminated ·Medtronic, Inc.·March 17, 2003

    Nonin Model 2500 PalmSAT handheld pluse Oximeter , Nonin Medical, Inc., Plymouth, MN USA

    FDA Recall
    Terminated ·Nonin Medical, Inc·Product code DQA·October 11, 2007

    Trep-Chek Syphilis Test Kit, 960 tests, Catalog No. TP-960, Distributed by DiaSorin, Inc. 1951 Northwestern Ave, Stillwater, MN 55082-0285 USA. Manufactured by Phoenix Bio-Tech Corp., 6910 Kitimat Road, Unit #1, Mississauga, Ontario, Canada L5N 5M2.

    FDA Recall
    Terminated ·Diasorin Inc.·Product code LIP·March 16, 2005

    Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement. Do not reuse. Ethylene Oxide Sterilized. Made in the U.S.A. Synovis Surgical Innovations A division of Synovis Life Technologies, Inc., 2575 University Ave. W., St. Paul, MN 55114-1024 USA.

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·November 1, 2005

    Quickie brand Freestyle M11 & F11, C. G. Tilt, Powered Wheelchair; Product is manufactured and distributed by Sunrise Medical, 2842 Business Park Ave., Fresno, CA 93727

    FDA Recall
    Terminated ·Sunrise Medical Inc·Product code ITI·November 15, 2005

    Eye surgery stretcher with crank fowler, model 1069 Stryker Medical 3800 E. Centre Ave Portage MI 49002. Intended use: A stretcher used for eye surgery.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FNJ·February 26, 2010

    Eye surgery stretcher with crank fowler, model 1079 Stryker Medical 3800 E. Centre Ave Portage MI 49002. Intended Use: A stretcher used for eye surgery.

    FDA Recall
    Terminated ·Stryker Medical Div. of Stryker Corporation·Product code FNJ·February 26, 2010

    Minstrel Patient Lift with SR weighing scale; a non-AC-powered patient lift; Arjo, Inc., 50 N. Gary Ave., Roselle, IL 60172; model number HMB002-US

    FDA Recall
    Terminated ·Arjo, Inc.·Product code FNG·August 31, 2006