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U.S. Department of Health and Human Services

Enforcement Report - Week of March 6, 2013

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Product Detail

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
Recall Number D-178-2013
Classification Class II
Code Info Lot #: C201028, Exp 12/13
Product Distributed Qty 27,805 bottles
Reason For Recall Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

Event Detail

Event Id 63285
Product Type Drugs
Status Ongoing
Recalling Firm Dr. Reddy's Laboratories, Inc.
City Bridgewater
State NJ
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-08-01
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide