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Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-132...

FDA Recall #D-103-2013 — Class II — July 25, 2012

Recall #D-103-2013 Date: July 25, 2012 Classification: Class II Status: Terminated

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.

Reason for Recall

Subpotent; 9-month stability interval

Recalling Firm

Lloyd Inc. of Iowa — Shenandoah, IA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

16,548/100-tablet bottles

Distribution

Distribution was nationwide and to Puerto Rico. There was no foreign, military, or government distribution.

Code Information

Lot 1094098, exp. date 9/2012

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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