PlainRecalls
FDA Drug Moderate Class II Terminated

Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-344-30

Reported: March 6, 2013 Initiated: August 1, 2012 #D-180-2013

Product Description

Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-344-30

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
48, 754 bottles (C108376)/47,520 bottles (C108634)
Distribution
Nationwide
Location
Bridgewater, NJ

Frequently Asked Questions

What product was recalled?
Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-344-30. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 48, 754 bottles (C108376)/47,520 bottles (C108634).
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-180-2013.