Actavis Totowa LLC, a generic drug manufacturer has voluntarily recalled all drug products manufactured at its Little Falls, New Jersey facility. This was a precautionary, voluntary action by Actavis following an inspection conducted by the Food and Drug Administration earlier this year. The inspection at Little Falls revealed operations which did not meet the FDA's or Actavis' standards for good manufacturing practices. Recall letters have been issued to wholesalers and retailers, instructing them to return product to Capital Returns, Milwaukee, WI. Actavis Totowa, LLC is a United States subsidiary of Actavis Group hf. This voluntary action was limited only to the Actavis Totowa products manufactured in the Little Falls, NJ facility listed below. Products manufactured by Actavis Elizabeth LLC, Actavis South Atlantic LLC, Actavis Mid Atlantic LLC or Actavis products manufactured in other facilities are thus not impacted by this recall.