BEUDAMED
    56 results · 26ms · 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 ×

    Angiotech***Custom General Biopsy Tray for OMA North of Oklahoma City*** 1 - 60cc Syringe; 2 - 10cc Syringe L/L; 1 -18ga x 1-1/2" Needle; 1 - 19ga x 1-1/2" Filter Needle; 1 - 20ga x 1-1/2" Needle; 1 - 21ga x 1-1/2" Needle; 1 - 25ga x 5/8" Needle; 1 - 50cm Extension Tube; 1 - 10% Povidone Iodine Swab Sticks (3Pkg); 1 - 1% Lidocaine (5mL); 1 - 3" x 3" Sponges is stacks of 5 (4-Ply); 1 - Fenestrated Drape; 1 - Towel; 1 - CSR Wrap***Catalog Number: CG0072***Sterile - For single patient use. STERILE EO. Caution: Federal (USA) Law restricts this device to sale by or on the order of a physician. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 SW Ave. Gainesville, FL 32808 U.S.A. Domestic: 877-991-1110, International: 732-626-6466, [email protected], www.angiotech.com. Intended for the purpose of harvesting bone and/or bone marrow specimens.

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code OJV·December 22, 2010

    Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: No

    FDA Recall
    Open, Classified ·Natus Neurology DBA Excel Tech., Ltd. (XLTEK)·Product code OMA·May 7, 2025

    Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a short-term neurological monitoring system that collects, displays, and stores multiple physiological measurements Model: CNS-350

    FDA Recall
    Open, Classified ·Moberg Research, Inc.·Product code OMA·February 20, 2023

    natus newborn care Olympic Brainz Monitor, REF OBM00002. electroencephalograph

    FDA Recall
    Terminated ·Natus Neurology DBA Excel Tech., Ltd. (XLTEK)·Product code OMA·March 5, 2020

    VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.

    FDA Recall
    Open, Classified ·LivaNova USA Inc·Product code LYJ·February 4, 2020

    Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053

    FDA Recall
    Open, Classified ·AtriCure, Inc.·Product code GEH·November 28, 2023

    Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056

    FDA Recall
    Open, Classified ·AtriCure, Inc.·Product code GEH·November 28, 2023

    3M Micropore Paper Tape, Cat. No. 1530-154, 1 in x 54 in., 800 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Paper Tape, Cat. No. 1530-15Y, 1 in x 5YDS., 441 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Paper Tape, Cat. No. 1530-336, 3 in x 36 in., 240 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Paper Tape, Cat. No. 1530-136, 1 in x 36 in., 800 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Paper Tape, Cat. No. 1530-118, 1 in x 18 in., 800 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Paper Tape, Cat. No. 1530-12Y, 1 in x 2YDS., 630 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Paper Tape, Cat. No. 1530-254, 2 in x 54 in., 400 rolls / case.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    3M Micropore Single Use Rolls, Surgical Tape, REF 1530S-1, 1 in x 1-1/2 yd.

    FDA Recall
    Terminated ·Product code KGX·January 29, 2010

    TRUE Dilatation Balloon Valvuloplasty Catheter, REF Numbers: 02045-11, 02245-12, 02445-12, and 02645-13; Sizes: 20mm x 4.5cm, 22mm x 4.5cm, 24mm x 4.5cm, and 26mm x 4.5cm; Intended to be used for balloon aortic valvuloplasty.

    FDA Recall
    Terminated ·Loma Vista Medical·Product code OZT·March 18, 2013

    LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal tube or esophageal/tracheal double lumen tube. This device is to be used as an adjunct to assess intubation. Its purpose is not to eliminate clinical judgment

    FDA Recall
    Terminated ·LMA North America Inc·Product code BTR·May 23, 2012

    LMA- Unique Laryngeal Mask Airway Size 4, Catalog No. 12140, Lot FH041202 Size 4, Catalog No. 12150, Lot FJ021202

    FDA Recall
    Terminated ·LMA North America Inc·Product code CAE·June 18, 2003

    Curix Opthos H, size 35x43 cm A radiographic medical x-ray film designed to optimize diagnostic chest imaging by providing complete diagnostic information including superbly visualized lung detail along with a high level of retro-cardiac, sub-diaphragmatic and mediastinal information.

    FDA Recall
    Terminated ·AGFA Corp.·Product code IWZ·October 4, 2011

    Magellan Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881850558

    FDA Recall
    Terminated ·Cardinal Health·Product code FMI·February 9, 2021