PlainRecalls
FDA Drug Moderate Class II Terminated

Dr. Reddy's Ciprofloxacin Tablets, USP 500 mg*, 500 Tablets, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-127-05

Reported: August 8, 2012 Initiated: April 9, 2012 #D-1435-2012

Product Description

Dr. Reddy's Ciprofloxacin Tablets, USP 500 mg*, 500 Tablets, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-127-05

Reason for Recall

Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets

Details

Units Affected
1656 bottles
Distribution
Nationwide and Puerto Rico
Location
Bridgewater, NJ

Frequently Asked Questions

What product was recalled?
Dr. Reddy's Ciprofloxacin Tablets, USP 500 mg*, 500 Tablets, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325 INDIA, NDC 55111-127-05. Recalled by Dr. Reddy's Laboratories, Inc.. Units affected: 1656 bottles.
Why was this product recalled?
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets
Which agency issued this recall?
This recall was issued by the FDA Drug on August 8, 2012. Severity: Moderate. Recall number: D-1435-2012.