The FDA issued an advisement to health care professionals not to use any liquid products manufactured by PharmaTech LLC, in Davie, Fla., due to Burkholderia cepacia contamination and the potential for severe patient infection.
Rugby Laboratories, in Livonia, Mich., announced a voluntary recall on Aug. 3, 2017, of two such products—Diocto Liquid and Diocto Syrup, both oral liquid docusate products—manufactured by PharmaTech.