FDAClass IIMarch 6, 2013

Citalopram tablets USP recall: Contamination

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

Why was Citalopram tablets USP recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: C108376, C108634, Exp 11/13

Product
Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-344-30
Recalling firm
Dr. Reddy's Laboratories, Inc.
Quantity
48, 754 bottles (C108376)/47,520 bottles (C108634)
Distribution
Nationwide
Recall date
March 6, 2013
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls