Home / Brands / Inari Medical - Oak Canyon
Inari Medical - Oak Canyon Recalls
2 recalls on record · August 28, 2024 to May 14, 2025 · Medical Devices
Recalls by year
24
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 14, 2025Medical DevicesFDA
Inari Medical - Oak Canyon recalls Artix MT Thrombectomy Device, REF: 32-102
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.
August 28, 2024Medical DevicesFDA
Inari Medical - Oak Canyon recalls ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thromb
Hazard: Thrombectomy system catheter instructions for use updated to reduce adverse events due to the following circumstances: 1) Fibrous, firmly adherent, calcified material, or suspected tumor thrombus overloading catheter bag 2) Catheter pulled through internal jugular vein access site or not pulled away from heart; may lead to device entrapment, pulmonary embolism, venous cutdown, abdominal surgery.