Lloyd Inc recalls Levothroid (levothyroxine sodium tablets, USP), 50 mcg., packaged in 100-ct. bottles, RX, NDC 0456-1321-01. Manufacture
Recalled July 4, 2012 · FDA recall D-1393-2012 · Lloyd
Hazard
Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval. · FDA Class II
Units
19,166 bottles
Sold at
Nationwide and PR.
Description
Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Product
Levothroid (levothyroxine sodium tablets, USP), 50 mcg., packaged in 100-ct. bottles, RX, NDC 0456-1321-01. Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
Manufacturer(s)
Lloyd Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →