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
- Company
- Dr. Reddy'S Laboratories, Inc.
- Recall Initiated
- August 1, 2012
- Posted
- March 6, 2013
- Recall Number
- D-180-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 48, 754 bottles (C108376)/47,520 bottles (C108634)
- Firm Location
- Bridgewater, NJ, United States
Reason for Recall
Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
Distribution
Nationwide
Lot / Code Info
Lot #: C108376, C108634, Exp 11/13
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