Working with FDA, Standard Homeopathic Company Voluntarily Recalls Hyland s Teething
Working with FDA, Standard Homeopathic Company Voluntarily Recalls Hyland s Teething Tablets to Address Manufacturing Process
Standard Homeopathic Company, in consultation with the U.S. Food and Drug Administration (FDA), is voluntarily recalling its Hyland s Teething Tablets. The company is initiating this recall in an abundance of caution due to an FDA investigation of its manufacturing facility. Hyland s Teething Tablets are manufactured in the United States and distributed throughout North America.
Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h
Actavis Inc. today announced a voluntary recall to the wholesale and retail levels only of 18 lots of Fentanyl Transdermal System 25 mcg/hour C-II patches manufactured for Actavis by Corium International in the United States. Actavis identified one lot of 25 mcg/hour Fentanyl patch(Control/Lot # 30349) shipped to market that contained one patch that released its active ingredient faster than the approved specification in laboratory testing.