Drug recall
Artix MT Thrombectomy Device, REF: 32-102
FDA recall event 96682 · Class II · Inari Medical - Oak Canyon
Key facts
| Event ID | 96682 |
|---|---|
| Recall numbers | Z-1728-2025 |
| Recalling firm | Inari Medical - Oak Canyon |
| Product type | Devices |
| Products | Artix MT Thrombectomy Device, REF: 32-102 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Apr 8, 2025 |
| Report date | May 14, 2025 |
| City | Irvine |
| State | CA |
| Country | United States |
| FEI number | 3020347218 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: