Home › Inari Medical, Inc. › Artix MT

Artix MT

Inari Medical, Inc. · Model 32-102 / AS-01248 · UDI-DI 00810123710584

KRA DQY DYB Prescription

510(k) clearances

9,137

Adverse events (366 deaths)

137

Recalls

150

Facilities

Description

Artix MT (Thrombectomy Device)

Recalls

Date	Firm	Reason
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16	Boston Scientific Cork, Ltd.	The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.