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Synthroid (levothyroxine sodium) Tablets USP, 50 mcg, Rx Only, 90-Count Bottle, Abbott Laboratori...

FDA Recall #D-1694-2012 — Class II — July 19, 2012

Recall #D-1694-2012 Date: July 19, 2012 Classification: Class II Status: Terminated

Product Description

Synthroid (levothyroxine sodium) Tablets USP, 50 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-4552-90.

Reason for Recall

Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.

Recalling Firm

Abbott Laboratories — Abbott Park, IL

Classification

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

Product Type

Drugs

Product Quantity

53,448 Bottles

Distribution

Nationwide

Code Information

18265A8, Exp 09/20/2013

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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