Lloyd Inc. of Iowa recalls Levothroid (levothyroxine sodium tablets, USP), 137 mcg., 100-count bottles, Rx only, NDC 0456-1331-01, Manufactured f
Recalled December 12, 2012 · FDA recall D-083-2013 · Lloyd Inc. of Iowa
Hazard
cGMP Deviations; does not meet in process specification requirements · FDA Class II
Units
36,978/100-tablet bottles
Sold at
Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution.
Description
cGMP Deviations; does not meet in process specification requirements
Product
Levothroid (levothyroxine sodium tablets, USP), 137 mcg., 100-count bottles, Rx only, NDC 0456-1331-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
Manufacturer(s)
Lloyd Inc. of Iowa
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →