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U.S. Department of Health and Human Services

Enforcement Report - Week of January 2, 2013
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Product Detail

Product Description 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.
Recall Number D-101-2013
Classification Class II
Code Info Lot 1093992 and 1094095, exp. date 9/2012
Product Distributed Qty 37,441/100-tablet bottles
Reason For Recall Subpotent; 9-month stability interval

Event Detail

Event Id 62664
Product Type Drugs
Status Ongoing
Recalling Firm Lloyd Inc. of Iowa
City Shenandoah
State IA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-07-25
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution Pattern Distribution was nationwide and to Puerto Rico. There was no foreign, military, or government distribution.
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