Boston Scientific issues software correction for 3,592 pacemakers and cardiac devices
The FDA says Boston Scientific has opened a worldwide correction for software used in certain ACCOLADE-family pacemakers and CRT-P devices.
Boston Scientific
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FDA opens early alert for Boston Scientific percutaneous catheter issue
The FDA listed an early alert on July 24, 2026, involving a Boston Scientific percutaneous catheter and said it was collecting additional information.