Fda Medical Device Safety Communications On Tubing And Luer Misconnections

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Examples of Medical Device Misconnections | FDA

https://www.fda.gov/medical-devices/medical-device-connectors/examples-medical-device-misconnections

IV tubing erroneously connected to trach cuff. A child in a pediatric intensive care unit had both an IV line and a trach tube. The IV tubing was mistakenly connected …

FDA Activities: Medical Device Connectors | FDA

https://www.fda.gov/medical-devices/medical-device-connectors/fda-activities-medical-device-connectors

Safety Communications | FDA

https://www.fda.gov/medical-devices/medical-device-safety/safety-communications

Listing of Medical Device Safety Communications to describe FDA’s analysis of a current issue and provide specific regulatory approaches and clinical …

Tips for Health Care Providers to Reduce Medical …

https://www.fda.gov/medical-devices/medical-device-connectors/tips-health-care-providers-reduce-medical-device-misconnections

Consider the following actions to help prevent misconnections: During initial use, check new devices and equipment to identify potential misconnections and take immediate …

Medical Device Connectors | FDA

https://www.fda.gov/medical-devices/general-hospital-devices-and-supplies/medical-device-connectors

Patients in health care settings receive food, medication and other therapies through a variety devices, or delivery systems, such as syringes, catheters, and tubing sets that …

www.fda.gov/cdrh/luer CASE STUDIES - Food and …

https://www.fda.gov/media/75542/download

the serious problem of tubing misconnections,” said ... More Patient Deaths from Luer Misconnections. October 2007. ... The 2009 FDA Safe Medical Device Safety Calendar

Additional Resources: Medical Device Connectors | FDA

https://www.fda.gov/medical-devices/medical-device-connectors/additional-resources-medical-device-connectors

2010 Letter from FDA to manufacturers of enteral feeding tubes (PDF - 27KB) ISO 80369-1:2018 Small-bore connectors for liquids and gases in healthcare applications …

Reducing Risks through Standards Development for …

https://www.fda.gov/medical-devices/medical-device-connectors/reducing-risks-through-standards-development-medical-device-connectors

ISO 80369-6:2016, was published in March 2016, to provide specifications for designing connectors for use with neuraxial devices. The FDA recognizes this standard. …

Preventing Tubing and Luer Misconnections - fda.report

https://fda.report/media/83405/Preventing-%20Tubing-and-Luer-Misconnections.pdf

ACT to prevent tubing misconnections! To help reduce risk to patients, consider the following strategies, based on recommendations from The Joint Commission and ECRI …