Sorry, you need to enable JavaScript to visit this website.
Skip to main content
Regulation

Safety considerations to mitigate the risks of misconnections with small-bore connectors intended for enteral applications.

Rockville, MD: Center for Devices and Radiological Health, US Food and Drug Administration; February 11, 2015.

Save
Print
March 4, 2015
Rockville, MD: Center for Devices and Radiological Health, US Food and Drug Administration; February 11, 2015.

Mistakes due to small-bore Luer connector similarities can contribute to patient harm. This guidance provides ways for manufacturers, policy makers, and product designers to prevent misconnections, including recommendations regarding improvements for labeling, user testing, and risk assessment.

Save
Print
Cite
Citation

Rockville, MD: Center for Devices and Radiological Health, US Food and Drug Administration; February 11, 2015.

Related Resources From the Same Author(s)
Related Resources