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.
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