Valiant NavionRecalls & reported problems across all models
Medtronic, Inc. · 137 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Valiant Navion models — page 2
137 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Valiant Navion™ VNMF3434C229TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT5 reports
- Valiant Navion™ VNMC4343C218TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death5 reports
- Valiant Navion™ VNMC3131C90TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death5 reports
- Valiant Navion™ VNMC3434C90TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT5 reports
- Valiant Navion™ VNMC3737C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death5 reports
- Valiant Navion™ VNMF2828C97TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT4 reports
- Valiant Navion™ VNMF4646C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death4 reports
- Valiant Navion™ VNMF4034C185TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death4 reports
- Valiant Navion™ VNMF4640C185TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 deaths4 reports
- Valiant Navion™ VNMC3131C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death4 reports
- Valiant Navion™ VNMC3434C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT4 reports
- Valiant Navion™ VNMF2222C96TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death3 reports
- Valiant Navion™ VNMF4343C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death3 reports
- Valiant Navion™ VNMC2222C94TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT3 reports
- Valiant Navion™ VNMC4646C218TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death3 reports
- Valiant Navion™ VNMF2822C173TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death2 reports
- Valiant Navion™ VNMC2822C207TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death2 reports
- Valiant Navion™ VNMF3737C229TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death2 reports
- Valiant Navion™ VNMF4640C185TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death2 reports
- Valiant Navion™ VNMC2222C94TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death2 reports
- Valiant Navion™ VNMC4040C218TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 reports
- Valiant Navion™ VNMC3428C207TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 reports
- Valiant Navion™ VNMC4034C200TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death2 reports
- Valiant Navion™ VNMF3131C229TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Valiant Navion™ VNMF4646C103TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMC2525C94TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMF2525C96TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Valiant Navion™ VNMF3131C97TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMF3434C97TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMF4040C103TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMF4343C103TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Valiant Navion™ VNMF4343C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMF4034C185TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMC2828C90TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMC3131C223TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMC4040C95TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Valiant Navion™ VNMC4343C218TUSYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page