The Recall Desk
ModerateFDA (Drugs)·D-178-2013·Announced 2013-03-06

Dr. Reddy's Recalls Citalopram Tablets Due to Chemical Odor Complaints

Dr. Reddy's is recalling 27,805 bottles of Citalopram tablets 10mg due to reports of a strong garlic or chemical smell.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves chemical contamination (odor) without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Dr. Reddy's Laboratories, Inc. is recalling 27,805 bottles of Citalopram tablets USP, 10mg, 30-count. The affected product is identified by Lot # C201028 and an expiration date of 12/13. The recall is being conducted due to complaints reporting a strong garlic odor or strong chemical smell associated with the product.

The recalled medication was distributed nationwide. The product is a prescription-only medication manufactured by Dr. Reddy's Laboratories Limited in Bachupalli, India. The NDC number for the affected product is 55111-342-30.

Consumers and healthcare providers should check their inventory for this specific lot number and expiration date. If the product is found, it should be returned to the pharmacy or point of purchase for a refund or replacement. Patients should consult their healthcare provider for alternative treatment options if they are currently taking this medication.

The recalled product

Product
Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-342-30
Manufacturer
Dr. Reddy's Laboratories, Inc.
Category
Drug — Prescription Medication
Hazard
Affected units
27,805

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot #: C201028
  • Exp 12/13

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 3 recalled by Dr. Reddy's Laboratories, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

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