Baxter Healthcare Corporation, Automix Automated Nutrition Compounder Systems: Class I Recall – Risk of Fluid Entry into Device Keypads

by admin on August 29, 2012

A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Baxter Healthcare Corporation, Automix Automated Nutrition Compounder Systems: Class I Recall – Risk of Fluid Entry into Device Keypads. According to the Food & Drug Administration FDA’s MedWatch:

Large variations in dosing of critical components in highly vulnerable patients could lead to serious injury and/or death.

For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Baxter Healthcare Corporation, Automix Automated Nutrition Compounder Systems: Class I Recall – Risk of Fluid Entry into Device Keypads.

To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.

If you have thoughts on the drug or medical device recall or safety alert, share your drug or medical device recall or safety alert comments below.

Share Your Recall Comments Below!

    What Do You Think? Share Your Recall Comments!

    Previous post:

    Next post: