Some U.S. health regulators who review medical devices and tobacco products for safety and efficacy are struggling to meet ...

KUALA LUMPUR: The Medical Device Authority (MDA) received 48 complaints about the sale, advertising and marketing of unlicensed optical devices and contact lenses since the ban on online sales ...

The Subcommittee on Oversight and Investigations for the House Committee on Energy and Commerce raised concerns about ...

Medtronic has issued a recall for several aortic root cannula devices due to a potential safety risk that could cause loose material to dislodge during use, potentially leading to stroke or death. The ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering.