FDASeptember 18, 2019device

iLab Polaris Multi-Modality Guidance System; iLab Ultrasound Imaging System

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Completed

Brands named

boston scientificboston

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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iLab Polaris Multi-Modality Guidance System; iLab Ultrasound Imaging System — Recall Details · AllClear