FDAFDA · Food and drugs·Recall number D-1393-2012
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.
Published July 4, 2012 · Recall initiated: February 3, 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 (Single Ingredient Drug): Low assay at the 9-month test 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
- Distributor
- Nationwide and PR.
- Lot
- Lot 1087589
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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