Avea Ventilator Recall Issued Due to Sensor Problems
An Avea Ventilator Recall has been classified as Class I after reports of problems at high altitudes.
An Avea Ventilator Recall has been classified as Class I after reports of problems at high altitudes.
Defective motors have led to the recall of Carefusion Alaris drug infusion pumps, which federal regulators indicate could cause serious injury or death.
Federal regulators are have determined that a recalled infant ventilator system sold by CareFusion poses a substantial risk of serious injury or death for children.