The U.S. Food and Drug Administration is advising consumers and health care professionals not to use any liquid drug or dietary supplement products manufactured by PharmaTech LLC of Davie, Florida, and...

PharmaTech, LLC announced a voluntary recall all liquid products from October 20, 2015 through July 15, 2016 as a precautionary measure due to a potential risk of product contamination with Burkholderia...

In a follow-up to the Burkholdera cepacia, or B. cepacia outbreak linked to liquid docusate products, the Centers for Disease Control and Prevention (CDC) reported an additional nine cases in the past...

Officials with the U.S. Food and Drug Administration is alerting health care professionals that PharmaTech LLC, Davie, Florida, is voluntarily recalling all non-expired lots of Diocto Liquid, a docusate...

The Centers for Disease Control and Prevention (CDC) reported an additional six infections caused by Burkholderia cepacia complex Thursday, bringing the outbreak total to 53 in five states, At this time,...

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In a follow-up to reports last month that the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA) were investigating a multistate outbreak of Burkholderia cepacia...

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In an follow-up on the previous report on a multi-state outbreak of Burkholderia cepacia infections possibly linked to liquid docusate products, the Centers for Disease Control and Prevention (CDC) issued...

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The Centers for Disease Control and Prevention (CDC) is collaborating with the Food and Drug Administration (FDA), multiple state and local health departments, and numerous healthcare facilities to investigate...