FDAFDA · Food and drugs·Recall number D-101-2013
Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
Published January 2, 2013 · Recall initiated: July 25, 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
Subpotent; 9-month stability interval
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Lloyd Inc. of Iowa
- Distributor
- Distribution was nationwide and to Puerto Rico. There was no foreign, military, or government distribution.
- Lot
- Lot 1093992 and 1094095, exp. date 9/2012
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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