www.fdanews.com/articles/148898-fda-issues-class-i-recall-for-carefusion-infusion-pump-due-to-keypad-problems
FDA Issues Class I Recall for CareFusion Infusion Pump Due to Keypad Problems
August 23, 2012
U.S. health regulators announced a recall of CareFusion’s Alaris pump module Model 8100, saying a potential keypad malfunction in the infusion pump could cause serious injury or death.
MedCity News
MedCity News