Inari Medical - Oak Canyon
Inari Medical - Oak Canyon appears in FDA public data with 2 recalls — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1728-2025, Class II) was initiated on April 8, 2025.
Summary
- Total Recalls
- 2 (1 Class I)
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1728-2025 | Class II | Artix MT Thrombectomy Device, REF: 32-102 | April 8, 2025 |
| Z-2587-2024 | Class I | ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Cathete | July 19, 2024 |