Another CareFusion Infusion Pump Recall
The Food and Drug Administration (FDA) announced a Class I recall of the Model 8100 of the CareFusion 303 Alaris pump module due to a potential malfunction of the keypad that may cause death or injury to patients. A Class I recall is the most serious warning issued by federal regulators and is used if there is a risk of death or serious injury from a drug or other medical product. The FDA says that the