PROGRESS 1011844Recalls & reported problems
Abbott Vascular Inc. · HI-TORQUE PROGRESS 120 Guide Wire .014 Straight Tip 3.0 cm x 190 cm · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08717648138003), received between Mar 14, 2018 and Mar 14, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment Of Device Component” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Detachment Of Device Component1
- Difficult to Remove1
Patient problems
- Vessel Or Plaque, Device Embedded In1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 14, 2018Detachment Of Device Component; Difficult to Remove
IT WAS REPORTED THAT THE PROCEDURE WAS TO TREAT A HEAVILY CALCIFIED, HEAVILY TORTUOUS, 100% STENOSIS IN THE CHRONIC TOTAL OCCLUSION (CTO) IN THE DISTAL RIGHT CORONARY ARTERY (RCA). THE PROGRESS 120 GUIDE WIRE WAS ADVANCED TO THE DISTAL RCA; HOWEVER, THE GUIDE WIRE TIP BECAME STUCK IN THE CALCIFIED ANATOMY. DURING WITHDRAWAL OF THE GUIDE WIRE FROM THE ANATOMY, RESISTANCE WAS MET WITH THE ANATOMY AND THE DISTAL 3 CM OF THE TIP BECAME SEPARATED. THE SEPARATED TIP REMAINS STUCK IN THE CALCIUM. A SECOND PROGRESS 120 GUIDE WIRE WAS INSERTED, BUT THE PHYSICIAN DECIDED NOT TO PROCEED TO AVOID A SIGNIFICANT DELAY IN THE PROCEDURE. THERE WAS NO ISSUE WITH THE SECOND PROGRESS 120 GUIDE WIRE. THE PROCEDURE WAS ABORTED. THERE WAS NO ADVERSE PATIENT EFFECT. THERE WAS NO CLINICALLY SIGNIFICANT DELAY IN THE PROCEDURE. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Vessel Or Plaque, Device Embedded In
MAUDE report 7338667 ↗
Other WIRE, GUIDE, CATHETER devices
- HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II 1009664Abbott Vascular Inc. · WIRE, GUIDE, CATHETER321 reports
- SYNCHRO 14 M00313010Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls220 reports
- PressureWire™ C12059Lightlab Imaging, Inc. · WIRE, GUIDE, CATHETER1 death296 reports
- SYNCHRO 2 M00326410Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls155 reports
- ENROUTE .014" Guidewire 11686-01Silk Road Medical, Inc. · Wire, Guide, Catheter2 deaths228 reports
- ARROW IPN035915Teleflex Incorporated · WIRE, GUIDE, CATHETER217 reports
- OmniWire Pressure guide wire 89185Philips Image Guided Therapy Corporation · Wire, Guide, Catheter1 recall1 death160 reports
- ARROW IPN055780Teleflex Incorporated · Wire, guide, catheter4 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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