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Home » 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
