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Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories...

FDA Recall #D-178-2013 — Class II — August 1, 2012

Recall #D-178-2013 Date: August 1, 2012 Classification: Class II Status: Terminated

Product Description

Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-342-30

Reason for Recall

Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

Recalling Firm

Dr. Reddy's Laboratories, Inc. — Bridgewater, NJ

Classification

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

Product Type

Drugs

Product Quantity

27,805 bottles

Distribution

Nationwide

Code Information

Lot #: C201028, Exp 12/13

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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