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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:213396

Artix MT Thrombectomy Device, REF: 32-102

Official recall number

Z-1728-2025

Evidence summary

Product code
QEW
Recall status
Open, Classified
Event initiated
April 08, 2025
Root cause
Labeling Change Control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1728-2025

Field note

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