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Valiant Navion™ VNMC2828C90TU (UDI 00763000260743)Recalls & reported problems

Medtronic, Inc. · STENT GRAFT VNMC2828C90TU VAL NAV CS · Class 3 · Implant

All models of Valiant Navion (137)

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 00763000260743), received between Nov 26, 2020 and Nov 26, 2020 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Numbness1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 26, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    A VALIANT NAVION STENT GRAFT SYSTEM WAS IMPLANTED DURING AN UNKNOWN EMERGENT THORACIC ENDOVASCULAR PROCEDURE ON AN UNKNOWN DATE. IT WAS REPORTED, AN MRI TECHNICIAN CALLED TECHNICAL SERVICES TO REPORT THE PATIENT HAS REPORTED THAT THEY HAVE NO FEELING IN THEIR LEGS 4 DAYS AFTER THORACIC STENT GRAFT SURGERY. THERE IS NO OTHER ADDITIONAL INFORMATION AT THIS TIME.

    Patient problems: Numbness

    MAUDE report 10911092 ↗

Other SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT devices

All SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT devices →

Sources and updates

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