Drug Enforcement D-1394-2012

Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

Status

Terminated

Classification

Class II

Report Date

July 4, 2012

Termination Date

July 30, 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, Iowa 51601
Product quantity
19,039 bottles
Reason for recall
Subpotent (Single Ingredient Drug): Low assay at the 6-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

Location & Firm

Recalling firm
Lloyd Inc
Address
604 W Thomas Ave

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

Codes & Dates

Recall number
D-1394-2012
Event ID
61252
Recall initiation date
February 24, 2012
Center classification date
June 22, 2012
Code info
LOT NO.1092045
More code info
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