FDA recall D-180-2013

Dr. Reddy's Laboratories, Inc. · Class II · drug

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

Reason for recall

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

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2012-08-01
Report date
2013-03-06
Termination date
2013-05-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Bridgewater, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-180-2013