FDAFDA · Food and drugs·Recall number D-079-2013
Levothroid (levothyroxine sodium tablets, USP), 112 mcg., 100-count bottles, Rx only, NDC 0456-1330-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
Published December 12, 2012 · Recall initiated: July 9, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
cGMP Deviations; does not meet in process specification requirements
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Lloyd Inc. of Iowa
- Distributor
- Distribution was nationwide, including Puerto Rico. There was no foreign, military, or government distribution.
- Lot
- Lot #1096371, exp. 5/312013; and #1092299, exp. 1/31/2013
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States