FDAFDA · Food and drugs·Recall number D-178-2013
Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-342-30
Published March 6, 2013 · Recall initiated: August 1, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Dr. Reddy's Laboratories, Inc.
- Distributor
- Nationwide
- Lot
- Lot #: C201028, Exp 12/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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