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Medtronic Receives FDA Approval for Pipeline Flex Embolization Device with Shield Technology

Medtronic plc announced it has received approval from the United States Food and Drug Administration (FDA) for Pipeline Flex Embolization Device with Shield Technology.

CBET Announces Purdue Partnership at MD Expo

Purdue University is pairing its online courses to prepare health care professionals for the Certified Registered Central Service Technician exam with an externship program that gets them the 400 hours of experiential learning they must have to take the exam and become certified.

Avidicare Launches Opragon in a Box

Opragon In a Box is an all-in-one health care ventilation system that creates an ultra-clean zone for infection sensitive surgery.

EarthSafe Launches EvaClean Disposable Surface Disinfection Wipes

EarthSafe has enhanced its end-to-end infection prevention solution with the addition of the EvaClean Dry Wipes System.

GE Healthcare Recalls Carestation 600 Series Anesthesia Systems

GE Healthcare is recalling the Carestation 620/650/650c A1 anesthesia systems because there is a potential for a loose cable connection inside the system which may cause the mechanical ventilation to stop working. If this occurs, the system will emit a high priority audio and visual alarm to alert the health care provider. Loss of mechanical ventilation could lead to low (hypoxia) blood oxygen levels in the patient if the health care provider does not ventilate the patient manually or with an alternate system.

The use of the affected product may cause the patient to have low blood oxygen levels, which could result in tissue or organ damage, or death.

There were no reported injuries or deaths.

For more information, visit the FDA website.

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