279 results
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24ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Lunderquist -Ring Torque Wire Guide, Guidewire Reference Part Number/GPN THSF-35-125-THG G27031 THSF-35-145-THG G27033
FDA Recall
Open, Classified
·Cook Incorporated·Product code DQX·August 16, 2022
Torq-Flex Wire Guide Australian Modification, Guidewire Reference Part Number/GPN STF-18-40-AUST G07304
FDA Recall
Open, Classified
·Cook Incorporated·Product code DQX·August 16, 2022
Rosen Curved Wire Guide, Guidewire Reference Part Number/GPN THSCF-35-220-1.5-ROSEN G01623 THSCF-35-80-1.5-ROSEN G01774 THSCF-35-180-1.5-ROSEN G01264 THSCF-35-145-1.5-ROSEN G01261
FDA Recall
Open, Classified
·Cook Incorporated·Product code DQX·August 16, 2022
Heavy Double Flexible Tipped Wire Guide, Guidewire Reference Part Number/GPN: THDOC-35-60-0-3 G11949 C-HDOC-18-40-0-2 G09201 C-THDOC-18-40-0-2-HTS G26925
FDA Recall
Open, Classified
·Cook Incorporated·Product code DQX·August 16, 2022
Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874)
FDA Recall
Open, Classified
·Cook Incorporated·Product code DQX·August 16, 2022
COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792
FDA Recall
Open, Classified
·Cook Incorporated·Product code DQX·March 5, 2026
Platinum Plus" LT , REF 46-602, UPN M001466020, LT/0.018/260, Sterilized with ethylene oxide gas, Rx only, Legal Manufacturer Boston Scientific Corporation, One Boston scientific Place, Natick, MA 01760-1537, Made in USA: 8600 NW 41st Street, Miami, FL 33166-6202. The Platinum Plus" Guidewire facilitates placement of a catheter during diagnostic or interventional intravascular procedures. The wire can be torqued to facilitate navigation through tortuous arteries and/or avoid unwanted side branches.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code DQX·August 25, 2008
Merit Laureate Hydrophylic Guide Wire, Angled Stiff Shaft, Made In Ireland, CAT No: LWSTFA35260EX, 260cm, 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
Boston Scientific, Fathom"-14 Steerable Guidewire, Peripheral Vascular Use, 200 cm x 10 cm, REF 50-810, UPN M001508100 Sterilized with ethylene oxide gas, Rx Only, Made in 2405 Orion Circle, West Valley City, UT 84119 USA.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code DQX·June 3, 2010
Boston Scientific, Fathom"-14 Steerable Guidewire, Peripheral Vascular Use, Pre-Shaped 300 cm x 10 cm, REF 50-815, UPN M001508150 Sterilized with ethylene oxide gas, Rx Only, Made in 2405 Orion Circle, West Valley City, UT 84119 USA.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code DQX·June 3, 2010
Argon Medical Devices, ArgoGuide Hydrophilic NiTi Guidewire, Catalog Number: AG087311, .035/180 cm, stiff/angled/standard, sold as a single hydrophilic guidewire in bulk non-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: AG087306, .035/300 cm, regular/angled/standard, sold as a single hydrophilic guidewire in bulk non-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: AG387326, .032/150 cm, regular/angled/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: AG387302, .035/180 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: AG087303, .035/300 cm, regular/straight/standard, sold as a single hydrophilic guidewire in bulk non-sterile packaging. Argon Medical Devices, Inc. Athens, TX 75751.
FDA Recall
Terminated
·Argon Medical Devices, Inc·Product code DQX·February 26, 2009
Boston Scientific Fort Guide Wire, Floppy Marker Wire, 300cm x 2 cm, REF 34949-02, for use in intravascular interventional procedures.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code DQX·May 12, 2009
Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewire, Models ARCSJ200W, ARCSJ260W, and ARCDJ260W. Sterile using ethylene oxide. Product Usage: The Medtronic Archer 0.035 inch (0.89mm) Super Stiff Guidewires are intended to facilitate catheter placement and exchange during diagnostic or interventional procedures in the aorta, where increased support, distal flexibility, and low surface friction of the guidewire is needed.
FDA Recall
Terminated
·Medtronic Inc. Cardiac Rhythm Disease Management·Product code DQX·March 13, 2013
Radial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04020-RIHM
FDA Recall
Terminated
·Arrow International Inc·Product code DQX·April 11, 2018
Radial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
FDA Recall
Terminated
·Arrow International Inc·Product code DQX·April 11, 2018
Radial Arterial Access Kit; Product Code: ASK-04001-BID2
FDA Recall
Terminated
·Arrow International Inc·Product code DQX·April 11, 2018