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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:185929

Valiant Navion Thoracic Stent Graft System. For endovascular repair of lesions in the descending thoracic aorta (DTA).

Official recall number

Z-1201-2021

Evidence summary

Product code
MIH
Recall status
Open, Classified
Event initiated
February 12, 2021
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1201-2021