Key Takeaway

Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-342-30 by Dr. Reddy's Laboratories, Inc. was recalled on August 1, 2012. The hazard: Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.

FDA Drug Class II Terminated

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

Recalled: August 1, 2012 ~27,805 bottles units affected D-178-2013

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

Hazard / Reason

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

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

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

Drugs

Company Information

Dr. Reddy's Laboratories, Inc.

Bridgewater, NJ, United States

View all 163 recalls by Dr. Reddy's Laboratories, Inc. →

Distribution

Nationwide

Related Recalls

Frequently Asked Questions

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