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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:207795

ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft

Official recall number

Z-1999-2024

Evidence summary

Product code
DYF
Recall status
Open, Classified
Event initiated
May 03, 2024
Root cause
Equipment maintenance
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1999-2024

Field note

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