Recalls / Class II
Class IID-179-2013
Product
Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-343-30
- Affected lot / code info
- Lot #: C201922, Exp 1/14
Why it was recalled
Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.
Recalling firm
- Firm
- Dr. Reddy's Laboratories, Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 200 Somerset Corporate Blvd Fl 7th, N/A, Bridgewater, New Jersey 08807-2862
Distribution
- Quantity
- 86, 093 bottles
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2012-08-01
- FDA classified
- 2013-02-28
- Posted by FDA
- 2013-03-06
- Terminated
- 2013-05-24
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-179-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.