Inari Medical - Oak Canyon FDA Recalls

2 recalls on file across devices, 1 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Artix MT Thrombectomy Device, REF: 32-102Class IIApr 8, 2025Thrombectomy device specifies vessel range of 2.5-6 mm on th	Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather t	Class IIDevices	Apr 8, 2025
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever ThrombClass IJul 19, 2024Thrombectomy system catheter instructions for use updated to	Thrombectomy system catheter instructions for use updated to reduce adverse events due to the following circum	Class IDevices	Jul 19, 2024