BEUDAMED
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    Filters FDA Recall × Status: Terminated × Clear all

    AXIOM Artis dTA, Model Number 7008605

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code OWB·June 12, 2019

    Axiom Artis dTA, Axiom Artis Modular Angiography X-Ray System, Model number 7008605.

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code IZI·September 2, 2008

    AXIOM Artis System dTA using software version VB31D with 30x40 cm2 flat detectors. AXIOM Artis is a angiography system developed for single and biplane diagnostic imaging and interventional procedures.

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code IZI·August 25, 2008

    SOMATOM Definition AS, a family of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission dta from either the same axial plane taken at different angles or spiral planes taken at different angles.

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code JAK·March 22, 2016

    Model 6149 Pacing Vector Selector Cable Switch for use with Pacing System Analyzers * Rx only * Contents Are Not Sterile * Manufactured by Remington Medical Incorporated, 6830 Meadowridge Court, Alpharetta, GA 30005, (770) 888-8520 or (800) 999-0057 * Distributed By: Guidant Corporation, 4100 Hamine Avenue North, St. Paul, MN 55112-5798 USA.

    FDA Recall
    Terminated ·Remington Medical Inc.·Product code DTA·August 31, 2005

    Medtronic CapSureFix Novus Lead Model 5076.

    FDA Recall
    Terminated ·Medtronic Inc. Cardiac Rhythm Managment·Product code DTA·October 20, 2004

    Artis systems - Product Usage: an angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Model Numbers: System Material # AXIOM Artis FC 05904433; AXIOM Artis FA 05904441; AXIOM Artis MP 05904466; AXIOM Artis BC 05904649; AXIOM Artis BA 05904656; AXIOM Artis dBC Mag. Nav. 05917054; AXIOM Artis TA 07007755; AXIOM Artis dTA 07008605; AXIOM Artis dFC 07412807; AXIOM Artis dTC 07413078; AXIOM Artis dBA 07555357; AXIOM Artis dMP 07555365; AXIOM Artis dFA 07555373; AXIOM Artis dFC Mag. Nav. 07727717; AXIOM Artis TC 07728350; AXIOM Artis dBC 07728392; Artis zee floor 10094135; Artis zee ceiling 10094137; Artis zee MP 10094139; Artis zee biplane 10094141; Artis zee floor MN 10094142; Artis zee biplane MN 10094143; Artis Q floor 10848280; Artis Q ceiling 10848281; Artis Q biplane 10848282; Artis Q.zen floor 10848353; Artis Q.zen ceiling 10848354; Artis Q.zen biplane 10848355.

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc·Product code OWB·March 30, 2021

    Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery 1 (TA-UB1) is a rechargeable power source for the Thermal Angel Blood and IV Fluid Infusion Warmer. The TA-UB1 battery was designed to provide sufficient power for the Thermal Angel to warm and deliver one liter of blood or IV fluid infusion to a trauma patient.

    FDA Recall
    Terminated ·Estill Medical Technologies, Inc·Product code BSB·July 25, 2014

    Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #: 16-02-85, 120 v/60 Hz

    FDA Recall
    Terminated ·LivaNova USA·Product code DWC·April 20, 2018

    Estrogen Receptor AB-11 (Clone ID5) Mouse Monoclonal Antibody 1 mk (2mg.ml) Manufactured by: Lab Vision Corporation, Fremont, CA Thermo Fisher Scientific Anatomical Pathology Tudor Rd., Manor Park Rancorn, Cheshire WA7 1TA UK Analyte specific reagent. It is intended for qualitative immunohistochemistry with normal and neoplastic formalin-fixed, paraffin embedded tissue sections, to be viewed by light microscopy.

    FDA Recall
    Terminated ·Lab Vision Corporation·Product code MVU·December 6, 2013

    NPWT Small Mobile Bag No Logo; an adjunct to the MoblVac Portable Wound Care Pump; Ohio Medical Corporation, 1111 Lakeside Drive, Gurnee, IL 60031; Model 769709.

    FDA Recall
    Terminated ·Ohio Medical Corporation·Product code BTA·May 10, 2010

    Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal Aspiration Tubing is used with the Dominant Flex Surgical Suction Pump.

    FDA Recall
    Terminated ·Medela AG Medical Technology Lattichstrasse 4b Baai Switzerland·Product code BTA·December 2, 2020

    SSCOR Suction Device Model 2310V

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    SSCOR Suction Device Model 2310BV

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    Easy Go Vac Aspirator, Model PM65HG. Portable suction unit

    FDA Recall
    Terminated ·Precision Medical, Inc.·Product code BTA·November 9, 2004

    Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to aspirate saliva, mucous, vomitus or other aspirant from the mouth or airway to allow adequate respiration or ventilation of the patient.

    FDA Recall
    Terminated ·Ohio Medical Corporation·Product code BTA·August 14, 2018

    SSCOR Suction Device Model 2310BV-230

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    Suction Jar Lid for Medela Vario 18 Vacuum Pump used with the Bravo pH Monitoring System Medtronic Part Number: 9043K2101. (9043K2111 is the OUS version) The Vacuum Pump is used to provide the vacuum pressure during Capsule attachment. Correct Overflow lid: Medela CH-6341 Baar Switzerland Art. No. 077.0440, Small lid with conical patient connection 6-10mm and overflow protection device.(Incorrect overflow lid is Medela P/N: 077.0450)

    FDA Recall
    Terminated ·Medtronic Neuromodulation·Product code BTA·April 25, 2008

    NeoMedix Trabectome I/A Console, Model Number 550014, surgical aspirator

    FDA Recall
    Terminated ·Neomedix Corp·Product code BTA·May 28, 2007

    SSCOR Suction Device Model 2315

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005