DQA Update: FDA announces voluntary nationwide recall of all liquid products manufactured by PharmaTech and distributed by six companies

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DPH Information Update

Healthcare Associated Infections (HAI) Prevention Program

Note: This message is being forwarded to the DQA Notifications & Updates list. 


Update August 10, 2016

FDA released an updated statement including a voluntary recall of all of liquid products manufactured by PharmaTech and distributed by: Rugby, Major, Bayshore, Metron, Centurion, and Virtus.

Instructions and a product list are included in the announcements, which can be read at http://www.fda.gov/Drugs/DrugSafety/ucm511527.htm and http://www.fda.gov/Safety/Recalls/ucm515610.htm.

This issue remains under investigation. In addition to the above recall of all liquid products manufactured by PharmaTech, both FDA and CDC continue to recommend that clinicians and patients not use any brand of liquid docusate sodium product as a stool softener or for any other medical purpose.

To date, CDC has confirmed 60 cases from 8 states.