FDA Alerts

Class I Recall: Baxter Healthcare Corporation, Automix Automated Nutrition Compounder Systems

Baxter Healthcare Corporation (Baxter) has initiated a voluntary recall of its Automix Compounder (Automix) because of incorrect key press responses, caused by fluid entry into device keypads, and intermittent electrical failures. Fluids, such as

Fri Jul 13 2012By Other Author

Baxter Healthcare Corporation (Baxter) has initiated a voluntary recall of its Automix Compounder (Automix) because of incorrect key press responses, caused by fluid entry into device keypads, and intermittent electrical failures. Fluids, such as water, cleaning solutions, and nutrition source solutions, may enter into the keypad of the Automix control module and may cause the Automix to generate an incorrect device response to an Automix operator's key press. The intermittent electrical failures may cause the motors on the Automix to pump nutrition solution when not programmed to do so, or may cause the Automix to stop compounding before it has finished appropriately mixing the Total Parenteral Nutrition (TPN) Solution. Causes for the intermittent electrical failures have not been determined.

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