Search Results for: recall

Evaluating UDI Implementation

In 2007, Congress passed the Food and Drug Administration Amendments Act of 2007, which mandated the FDA to create a unique device identification (UDI) system to track and identify medical devices across the medical device life cycle—basical

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Committee Management II

This article follows the previous article on Committee Management, which appeared in the July 2012 issue of 24×7 and discussed the hospital Medical Equipment Committee. This article will continue on this topic and review the hospital’s Environment of Care (EC) Committee. The Environment of Care The biomedical/clinical engineering professional is usually a member or could […]

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