Providers advised to halt use, monitor patients, and report any complications with BioZorb devices to the FDA.

Further amendments aim to clarify the process for reporting medical device recalls to Health Canada and increase the robustness of this reporting. For example, for recalls initiated by the ...

The filing follows Exactech’s failure to settle product liability claims from about 2,600 patients in response to recalls of ...

A new process that consolidates machine learning algorithms with unique human-based expertise promises to improve the regulatory and approval process for new medical devices by reducing the recall ...

Patient advocates are hoping for change under new director Michelle Tarver, while industry groups look to build on former ...

Exactech, which is owned by private equity firm TPG, entered bankruptcy with $352 million in debt and a sale agreement that ...

THOUSANDS of motors face being recalled over fresh Dieselgate allegations – with 20 different car brands in the firing line.

The recently revised pre-trial schedule in the multidistrict litigation (MDL) against Exactech gives new plaintiffs more time ...

Further recalls could be afoot following an investigation into thousands of cars not previously subject to cheat device claims. According to The Times, 47 ...

Here are five FDA alerts and recalls from 2024 for orthopedic and spine specialists to know: ...

Several Govee space heater models sold on Amazon and TikTok are being recalled due to the potential for being fire and burn ...