Lloyd Inc recalls Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured fo
Recalled July 4, 2012 · FDA recall D-1394-2012 · Lloyd
Hazard
Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval. · FDA Class II
Units
19,039 bottles
Sold at
Nationwide
Description
Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Product
Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, Iowa 51601
Manufacturer(s)
Lloyd Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →