Inari Medical - Oak Canyon recalls Artix MT Thrombectomy Device, REF: 32-102
Recalled Product
Artix MT Thrombectomy Device, REF: 32-102
Hazard / Issue
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.
Issued by
FDA
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