FDA Issues Alert on Guidewire Recall

The U.S. Food and Drug Administration (FDA) has issued an alert that Boston Scientific Corp. is recalling RotaWire ‘Elite’ core wires. The RotaWire Elite Guidewire and wireClip Torquer Guidewire are part of the Rotablator Rotational Atheroctomy System, a device used to open narrow arteries and improve blood flow to the heart.

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