ACIST Recalls Kodama Intravascular Ultrasound Catheter Due to Risk of Broken O-Ring Pieces Flushing into Arteries During Use

Date: 03/17/21

ACIST Kodama Intravascular Ultrasound Catheter

Lots: 00233370, 00233371, 00233372, 00233373, 00233385

Distribution Dates: November 10, 2020 to January 14, 2021

Devices Recalled in the U.S.: 490

Date Initiated by Firm: January 18, 2021

USA-FDA Link:   https://www.fda.gov/medical-devices/medical-device-recalls/acist-recalls-kodama-intravascular-ultrasound-catheter-due-risk-broken-o-ring-pieces-flushing