GORE-TEX Vascular Graft VT07070LRecalls & reported problems
W. L. Gore & Associates, Inc. · VG THIN WALL 7MM X 70CM LINED · Class 2 · Implant
All models of GORE-TEX Vascular Graft (17)
Data updated Oct 18, 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 00733132615995), received between Apr 3, 2023 and Apr 3, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Complete Blockage” (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 18, 2026.
Most reported problems
Device problems
- Complete Blockage1
Patient problems
- Obstruction/Occlusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 3, 2023Complete Blockage; Complete Blockage
ON (B)(6) 2014, THIS PATIENT UNDERWENT TREATMENT FOR OCCLUSION DUE TO PERIPHERAL ARTERIAL DISEASE (PAD) IN WHICH A GORE-TEX® VASCULAR GRAFT WAS USED AS A BYPASS. THE PROXIMAL ANASTOMOSIS WAS AT THE COMMON FEMORAL ARTERY, THE DISTAL ANASTOMOSIS WAS AT THE TIBIAL-PERONEAL TRUNK BELOW KNEE. ON (B)(6) 2014, AN ADVERSE EVENT TERMED "THROMBOSIS OF THE GORE BYPASS" WAS IDENTIFIED. ON (B)(6) 2014, A THROMBECTOMY AND AN ENDARTERECTOMY OF THE GRAFT WAS PERFORMED. GRAFT PATENCY WAS RESTORED AT THE END OF THE PROCEDURE. THE PATIENT RECOVERY WAS DESCRIBED AS UNEVENTFUL. ON (B)(6) 2014, THE PATIENT WAS DISCHARGED TO HOME.
Patient problems: Obstruction/Occlusion
MAUDE report 16661939 ↗
Other PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER devices
- Cardioroot HEWROOT0030Intervascular Sas · Prosthesis, Vascular Graft, Of 6mm And Greater Diameter1 recall2 deaths13 reports
- FLIXENE SLIDER GDS 25058Atrium Medical Corporation · PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall13 reports
- ADVANTA SLIDER GDS 22114Atrium Medical Corporation · PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall11 reports
- Cardioroot HEWROOT0032Intervascular Sas · Prosthesis, Vascular Graft, Of 6mm And Greater Diameter1 recall2 deaths10 reports
- FLIXENE SLIDER GDS 25129Atrium Medical Corporation · PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall9 reports
- ADVANTA SLIDER GDS 22222Atrium Medical Corporation · PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall8 reports
- FLIXENE SLIDER GDS 25137Atrium Medical Corporation · PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall8 reports
- FLIXENE SLIDER GDS 25138Atrium Medical Corporation · PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER1 recall7 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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