Boston Scientific Corporation recalls iLab Polaris Multi-Modality Guidance System;
Recalled Product
iLab Polaris Multi-Modality Guidance System; iLab Ultrasound Imaging System
Hazard / Issue
Certain iLab Polaris Systems which were upgraded with a previous 2.10 software version (disk batch 629774) contained a bug in which only the True Color Secondary Capture (SC) format will archive Diastolic Hyperemia-Free Ratio data as intended. If either Multi-Frame UltraSound (US) or SC Image Storage formats are used, the DFR data will not be archived and the user will not be notified of this unexpected behavior.
Issued by
FDA
Distribution: OUS: Japan, Belgium, Denmark, France, Great Britain, and Spain. No U.S. consignees.