LOTUS Edge™

Aortic Valve System

Boston Scientific announced a global, voluntary recall of the LOTUS Edge™ Aortic Valve. This voluntary recall is related solely to the complexities of the delivery system and is not related to the implanted valve. At this time, there are no known safety concerns for patients who have the LOTUS Edge valve implanted. The valve continues to show clinically effective performance post implant.

While we have been pleased with the benefits the LOTUS Edge valve has provided to patients, we have been increasingly challenged by the intricacies of the delivery system required to allow physicians to fully reposition and recapture the valve. This led us to the difficult decision to discontinue the LOTUS Edge platform.

For Patients

If you are a patient with a LOTUS valve and have specific questions about your clinical care, please discuss with your doctor. 
See LOTUS Patient Information

For HCPs

For HCPs that would like more information, please contact your Boston Scientific sales representative. 
See LOTUS Instructions for Use and MRI Information
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