Recalls / Class II
Class IID-101-2013
Product
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.
- Affected lot / code info
- Lot 1093992 and 1094095, exp. date 9/2012
Why it was recalled
Subpotent; 9-month stability interval
Recalling firm
- Firm
- Lloyd Inc. of Iowa
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 604 W Thomas Ave, N/A, Shenandoah, Iowa 51601-1744
Distribution
- Quantity
- 37,441/100-tablet bottles
- Distribution pattern
- Distribution was nationwide and to Puerto Rico. There was no foreign, military, or government distribution.
Timeline
- Recall initiated
- 2012-07-25
- FDA classified
- 2012-12-21
- Posted by FDA
- 2013-01-02
- Terminated
- 2013-11-14
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-101-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.