BEUDAMED
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    Conformer - Medium with holes (Sterile)

    FDA Recall
    Terminated ·Gulden Ophthalmics·Product code HQX·November 29, 2002

    Boston Scientific brand Synchro2 0.14" Guide Wire, 300 cm, Soft; Boston Scientific Corporation: Made in 2405 West Orton Circle, West Valley City, UT 84119 Product is distributed by Boston Scientific Corporation, Fremont, CA The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures.

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code DQX·June 7, 2010

    ARTERIAL ACCESS TRAY/Product SKU (Code) MMC-04001-1. Arterial access tray for radial artery catheterization set

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQX·October 29, 2010

    Boston Scientific IQ Guide Marker Wire. Catalog No. 38951-010, 185 cm, Straight Tip, Single Pack. Catalog No. 38951-012, 185 cm, Straight Tip, 5 pack. Sterile EO. Manufactured for: Boston Scientific Corporation, One Boston Scientific Place, Natick, MN 01760 USA. Boston Scientific Guide Wires are steerable guide wires available in a variety of lengths and diameters. The distal tip is shapeable, or, alternatively, is available in a preshaped ''J'' tip.

    FDA Recall
    Terminated ·Boston Scientific·Product code DQX·May 30, 2006

    St. Jude Medical FAST-CATH Hemostasis Introducer 4F, REF 406709, Length 12 CM, Lot 4219 Max. Guidewire O.D. .038", 2010-01, Manufacture, St. Jude Medical, 14901 DeVeau place, Minnetonka, MN 55345-2126, Sterile EO. Used for the introduction of catheters into a vessel.

    FDA Recall
    Terminated ·St. Jude Medical·Product code DQX·August 17, 2009

    Merit Laureate Hydrophylic Guide Wire, Angled Stiff Shaft, Made In Ireland, CAT No: LWSTFA35180, 180cm, Sterile EO, Merit Medical Systems, Inc., South Jordan, UT 84095. Intended to facilitate the placement of devices during diagnostic and interventional procedures.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code DQX·June 28, 2010

    Fixed Core Wire Guide

    FDA Recall
    Terminated ·Cook Inc.·Product code DQX·October 13, 2017

    Coons Interventional Wire Guide

    FDA Recall
    Terminated ·Cook Inc.·Product code DQX·October 13, 2017

    Amplatz Stiff Wire Guide

    FDA Recall
    Terminated ·Cook Inc.·Product code DQX·October 13, 2017

    Newton Wire Guide

    FDA Recall
    Terminated ·Cook Inc.·Product code DQX·October 13, 2017

    RADIAL ARTERY CATHETERIZATION KIT with SHARPS SAFETY FEATURES/Product SKU (Code) HF-04020-1. Cardiovascular catheter wire guide

    FDA Recall
    Terminated ·Arrow International Inc·Product code DQX·October 29, 2010

    Boston Scientific brand Synchro.14" Guide Wire, 45 cm, tip; Boston Scientific Corporation: Made in 2405 West Orton Circle, West Valley City, UT 84119 Product is distributed by Boston Scientific Corporation, Fremont, CA The Synchro guidewire series is intended for general intravascular use, including neurovascular and peripheral vasculatures. It can be used to selectively introduce and position catheters and other interventional devices within the peripheral and neurovasculature. This device should be used only by physicians trained in percutaneous intravascular techniques and procedures.

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code DQX·June 7, 2010

    Abbott Vascular ACS .035 Torque Device Part Number : 1003279. For use in cardiac diagnostic or therapeutic procedures.

    FDA Recall
    Terminated ·Abbott Vascular·Product code DQX·January 7, 2011

    HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures.

    FDA Recall
    Terminated ·Nitinol Devices and Components, Inc.·Product code DQX·May 28, 2014

    HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD, Stiff Shaft, Straight Tip, 150 CM Length; Manufactured for Covidien, Plymouth, MN; Manufactured by: NDC Inc., Fremont, CA. Manufactured in Costa Rica The HydroFinity Hydrophilic guidewire facilitates the introduction and placement of catheters and interventional devices to the desired anatomical location during diagnostic or interventional procedures.

    FDA Recall
    Terminated ·Nitinol Devices and Components, Inc.·Product code DQX·May 28, 2014

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387308, .035/180cm, stiff/straight/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, K011905, Catalog Number: 00-AG387319, .038/150cm, stiff/straight/standard, sold as a single hydrophilic guidewire in both sterile and bulk non-sterile packaging configurations. Argon Medical Devices, Inc. Athens, TX 75751

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·November 19, 2007

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG387309, .035/300 cm, stiff/straight/standard, sold as a single hydrophilic guidewire in sterile packaging. Argon Medical Devices, Inc. Athens, TX 75751.

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·February 26, 2009

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG387314, .038/180 cm, regular/straight/standard, sold as a single hydrophilic guidewire in sterile packaging. Argon Medical Devices, Inc. Athens, TX 75751.

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·February 26, 2009

    Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG387301, .035/150 cm, regular/straight/standard, sold as a single hydrophilic guidewire in sterile packaging. Argon Medical Devices, Inc. Athens, TX 75751.

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code DQX·February 26, 2009