FDAApril 8, 2025device

Artix MT Thrombectomy Device, REF: 32-102

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.

What to do

FDA enforcement status: Ongoing

Brands named

inari medical oak canyoninariinari medical

UPCs

00810123710584

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Artix MT Thrombectomy Device, REF: 32-102 — Recall Details · AllClear