PlainRecalls
FDA Drug Moderate Class II Terminated

Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-343-30

Reported: March 6, 2013 Initiated: August 1, 2012 #D-179-2013

Product Description

Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-343-30

Reason for Recall

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

Details

Units Affected
86, 093 bottles
Distribution
Nationwide
Location
Bridgewater, NJ

Frequently Asked Questions

What product was recalled?
Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-343-30. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 86, 093 bottles.
Why was this product recalled?
Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 6, 2013. Severity: Moderate. Recall number: D-179-2013.