Status
Terminated
Drug Enforcement D-1393-2012
Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Classification
Class II
Report Date
July 4, 2012
Termination Date
July 30, 2013
Product Information
- Product description
- 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.
- Product quantity
- 19,166 bottles
- Reason for recall
- Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
- Recall initiation reason
- —
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Distribution pattern
- Nationwide and PR.
Location & Firm
- Recalling firm
- Lloyd Inc
- Address
-
604 W Thomas Ave, Po Box 130
United States - Voluntary / Mandated
- Voluntary: Firm initiated
- Status date
- —
Codes & Dates
- Recall number
- D-1393-2012
- Event ID
- 61094
- Recall initiation date
- February 3, 2012
- Center classification date
- June 22, 2012
- Code info
- Lot 1087589
- More code info
- —