Catheter For Crossing Total Occlusions
Cardiovascular · 21 CFR 870.1250
To facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including subchronic and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention, such as angioplasty, atherectomy or stent placement.
Recent MDR events
1,370 adverse event reports on file
- Crosser iQ UltrasonicJul 27, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01888
- Crosser iQ UltrasonicJul 27, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01915
- CROSSERJul 20, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01854
- CROSSER IQ ULTRASONICJul 16, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01825
- PIONEER PLUS CATHETERJul 14, 2026MalfunctionVolcano Corporation3008363989-2026-00120
- CROSSER IQ ULTRASONICJul 3, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01701
- CROSSERJul 3, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01710
- POWERWIRE RADIOFREQUENCY GUIDEWIREJun 30, 2026InjuryBaylis Medical Technologies Inc.3020968442-2026-00002
- CROSSER IQ ULTRASONICJun 23, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01603
- CROSSER IQ ULTRASONICJun 20, 2026MalfunctionBard Peripheral Vascular, Inc.2020394-2026-01576
Event type breakdown
Recalls
7 recall events for this product code
- Bard Peripheral Vascular IncOpen, ClassifiedJan 5, 2024
BD Recanalization System, REF: BDRECANSYSTEM
Recanalization systems may be in a manufacturing mode that allows the system to continuously run without the typical 30 second pauses, and 4-minute warning/5-minute restart required messages to indicate the ten-minute maximum catheter use time has been exceeded, which may increase the risk of the device overheating or breaking.
Z-0676-2024 · View FDA record ↗ - Ra Medical Systems, Inc.TerminatedJul 4, 2020
DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and delivery system, collectively the DABRA
A software issue was identified which could result in user or patient injury, or may adversely impact laser performance. It is possible that an unintended release of laser light (radiation) may occur, injuring the user or patient.
Z-2497-2020 · View FDA record ↗ - Volcano CorporationTerminatedSep 2, 2015
Volcano Pioneer Plus Re-Entry Catheter;
Due to a manufacturing defect, there is the possibility that a small wire could extend through the catheter shaft of the Pioneer Plus intravascular Ultrasound Guided Re-Entry Catheters.
Z-2718-2015 · View FDA record ↗ - Ra Medical Systems, Inc.TerminatedUnknown
DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in occlusive peripheral vascular disease.
Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury.
Z-0050-2021 · View FDA record ↗ - Ra Medical Systems, Inc.TerminatedUnknown
DABRA Laser (RA-308 Excimer Laser)
Due to footswitch not meeting required specification for protection from ingress of solids or liquids. If spilling of liquids near or on the footswitch, it may fail in the 'on' position and allow the laser to continue to lase.
Z-0569-2021 · View FDA record ↗ - Ra Medical Systems, Inc.TerminatedUnknown
Ra Medical Systems DABRA Catheter 5F (1.5mm), REF: 1222-5000-01, LOT: 18-090400-094, USE BY: 2019-09-24, MFR DATE: 2018-09-24, CE, Laser Radiation, STERILE (Gam
The firm has become aware there is a potential problem with its DABRA catheters resulting in higher catheter calibration failure rate due to the product shelf life is currently less than the labeled shelf life.
Z-2006-2020 · View FDA record ↗ - Ra Medical Systems IncTerminatedUnknown
The DABRA Laser (model RA-308) is designed to provide ultraviolet laser energy endovascularly through a catheter to occluded lesions in the peripheral arteries
Lasers/Catheters did not calibrate during set-up prior to use.
Z-2218-2019 · View FDA record ↗
Registered firms
65 firms currently registered for this product code
Lynx Medical Pennsylvania
ERIE, PA, US
C.r. Bard, Inc.
MADISON, GA, US
C.r. Bard, Inc.
Queensbury, NY, US
Synergy Health Ast, Llc
Saxonburg, PA, US
Cardinal Health Mexico 244 S De Rl De Cv
Ciudad Juarez Chihuahua, MX
Sterigenics U.s., Llc
Salt Lake City, UT, US
Isomedix Operations, Inc.
Minneapolis, MN, US
Cordis Us Corp.
Miami Lakes, FL, US
Cook Incorporated
Bloomington, IN, US
Sterigenics U.s., Llc
Queensbury, NY, US
Platinum Focus Group Ltd.
London London, City of, GB
Zylox-tonbridge Medical Technology Co., Ltd.
Hangzhou Zhejiang, CN
Viant As&o Holdings, Llc
LACONIA, NH, US
Limflow Inc.
Irvine, CA, US
C.r. Bard, Inc.
COVINGTON, GA, US
Spectranetics Corp.
Colorado Springs, CO, US
Nitinol Devices & Components Costa Rica, S. R. L.
El Coyol Alajuela, CR
Medtronic, Inc.
Plymouth, MN, US
Philips Electronics Ltd
Mississauga Ontario, CA
510(k) clearances
57 clearances for this product code
- AngioSafe, Inc.Sep 22, 2025
K252315 · Santreva-ATK Endovascular Revasculariztion Catheter
- Baylis Medical Technologies, Inc.Sep 11, 2025
K251158 · PowerWire® 14 Radiofrequency Guidewire Kit
- LimFlow, Inc.May 31, 2025
K251376 · LimFlow ARC
- Baylis Medical Technologies, Inc.Feb 28, 2024
K232562 · PowerWire Radiofrequency Guidewire Kit
- Soundbite Medical Solutions, Inc.Aug 28, 2023
K230159 · SoundBite® Crossing System XS Peripheral
- Avinger, Inc.Apr 25, 2023
K230594 · Tigereye ST CTO-Crossing Catheter
- Tractus Vascular, LLCJan 19, 2023
K221163 · Tunnel Crossing Catheter
- LimFlow, Inc.Aug 31, 2022
K221541 · LimFlow ARC