Drug Enforcement D-103-2013

Subpotent; 9-month stability interval

Status

Terminated

Classification

Class II

Report Date

January 2, 2013

Termination Date

November 14, 2013

Product Information

Product description
Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.
Product quantity
16,548/100-tablet bottles
Reason for recall
Subpotent; 9-month stability interval
Recall initiation reason
—
Initial firm notification
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.

Location & Firm

Recalling firm
Lloyd Inc. of Iowa
Address
604 W Thomas Ave, N/A

United States
Voluntary / Mandated
Voluntary: Firm initiated
Status date
—

Codes & Dates

Recall number
D-103-2013
Event ID
62664
Recall initiation date
July 25, 2012
Center classification date
December 21, 2012
Code info
Lot 1094098, exp. date 9/2012
More code info
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