FDAMarch 29, 2017device

Refinity Rotational Intravascular Ultrasound (IVUS) Catheter; Product number: 400-0200.289; Catalog number 89800. Cardiovascular: The REFINITY (or REFINITY ST) Rotational IVUS Catheter (REFINITY or REFINITY ST) is intended for the intravascular ultrasound examination of coronary arteries. Intrava...

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

The hazard

High complaint rates of kinking near the junction of the proximal shaft to telescope section of the catheter. Kinking could result in disruption of normal clinical workflow or loss of imaging.

What to do

FDA enforcement status: Terminated

Brands named

volcano

Recall history

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

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