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Risk Manager and Critical Care Medicine personnel are informed by the FDA that CareFusion Alaris PC Unit, Model 8015 is recalled because an error code may result in serious injury, including death. Background of CareFusion Alaris PC Unit, Model 8015 Alaris PC Unit, Model 8015, by CareFusion 303 Inc, is part of the Alaris electronic [...]

Critical Care Medicine and Risk Manager healthcare personnel are informed by the FDA that CareFusion EnVe Ventilators are recalled due to a potential leak in patient breathing circuit or system that can cause serious adverse events, including death. Background of CareFusion EnVe Ventilators CareFusion EnVe Ventilators are used for continuous breathing support for the care [...]

Anesthesiology and Risk Managers are informed by the FDA that CareFusion Airlife Infant Breathing Circuit is recalled because there is a risk of a leak in the closed ventilation system that may cause serious adverse events, including death. Background of CareFusion Airlife Infant Breathing Circuit The respiratory breathing circuits are used with a ventilator when [...]

The Food & Drug Administration has alerted all risk assessment managers, neurologists, and all other concerned medical professionals of the recall for CareFusion’s Nicolet Cortical Stimulator which has been identified to have various technical failures. Background of CareFusion Nicolet Cortical Stimulators The recalled products, Nicolet Cortical Stimulators are a product of CareFusion. They are used [...]