How many recalls does Dr. Reddy's Laboratories, Inc. have?

Recalert has 134 U.S. recalls on record for Dr. Reddy's Laboratories, Inc., published between August 8, 2012 and December 17, 2025.

Which agencies have handled Dr. Reddy's Laboratories, Inc. recalls?

Dr. Reddy's Laboratories, Inc. appears as the recalling firm in recalls from: FDA (134).

Recalls filed with 1 agency: FDA (134).

First recall on record: August 8, 2012. Most recent: December 17, 2025.

Risk classification: Class I: 4 · Class II: 65 · Class III: 65

Date	Agency	Product	Recall number
February 12, 2014	FDA	Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only …D-1080-2014	D-1080-2014
September 25, 2013	FDA	IBU (TM) IBUPROFEN Tablets, USP, 800 mg, 500 -count bottle,(NDC 55111-684-05) Rx only, Di…D-1042-2013	D-1042-2013
August 21, 2013	FDA	Ranitidine Hydrochloride Tablets, USP, 150 mg, OTC, a) Equate brand Maximum Strength Acid…D-884-2013	D-884-2013
March 6, 2013	FDA	Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Labor…D-179-2013	D-179-2013
March 6, 2013	FDA	Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Labor…D-180-2013	D-180-2013
March 6, 2013	FDA	Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Labo…D-178-2013	D-178-2013
November 28, 2012	FDA	Dr. Reddy's Quetiapine Fumarate Tablets, 25mg, Rx Only, 500 tablets. Mfd By: Dr. Reddy…D-059-2013	D-059-2013
August 8, 2012	FDA	Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, …D-1434-2012	D-1434-2012
August 8, 2012	FDA	Dr. Reddy's Ciprofloxacin Tablets, USP 500 mg*, 500 Tablets, Rx only, Mfd. By: Dr. Reddy'…D-1435-2012	D-1435-2012

How many recalls does Dr. Reddy's Laboratories, Inc. have?: Recalert has 134 U.S. recalls on record for Dr. Reddy's Laboratories, Inc., published between August 8, 2012 and December 17, 2025.
Which agencies have handled Dr. Reddy's Laboratories, Inc. recalls?: Dr. Reddy's Laboratories, Inc. appears as the recalling firm in recalls from: FDA (134).

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