SUN PHARMACEUTICAL INDUSTRIES INC: 126 recalls on record

Recalls filed with 1 agency: FDA (126).

First recall on record: July 17, 2013. Most recent: August 26, 2026.

Risk classification: Class I: 2 · Class II: 82 · Class III: 42

Most recent recalls

DateAgencyProduct
January 22, 2020FDASumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (627…D-0660-2020
June 26, 2019FDAAllergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release …D-1388-2019
February 6, 2019FDABromSite (bromfenac ophthalmic solution) 0.075%, 5 mL bottles, Rx Only, Distributed by : …D-0422-2019
January 30, 2019FDALOPERAMIDE HCL TABLETS USP, 2 mg, ANTI-DIARRHEAL, 24 caplets per carton, OTC, Distribute…D-0391-2019
January 16, 2019FDAVecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized,…D-0372-2019
December 26, 2018FDAAbsorica (Isotretinoin) Capsules 30 mg USP, 30 capsules (3x10 Prescription Packs) Rx onl…D-1207-2019
May 23, 2018FDARiomet (metformin hydrochloride oral solution), 500 mg/5 mL (16 fl. oz.), 473 mL plastic …D-0818-2018
February 21, 2018FDAAzelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray), 30 mL, Rx only, Dis…D-0417-2018
December 20, 2017FDARiomet (metformin hydrochloride) Oral Solution Cherry Flavored 500 mg /5 mL, 4 fl. oz. (N…D-0109-2018
May 31, 2017FDAChildren's Cetirizine Hydrochloride Chewable Tablets, 5 mg, 30-count bottle, Manufactured…D-0857-2017
May 17, 2017FDAOlanzapine Tablets, 2.5 mg, 1000-count bottles, Rx Only, Distributed by: Sun Pharmaceutic…D-0699-2017
May 17, 2017FDAOlanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-cou…D-0702-2017
May 17, 2017FDAOlanzapine Tablets, 10 mg, packaged in a) 30-count bottles (NDC 62756-554-83), b) 100-cou…D-0701-2017
May 17, 2017FDAOlanzapine Tablets, 7.5 mg, packaged in a) 30-count bottles (NDC 62756-553-83), b) 100-co…D-0700-2017
March 29, 2017FDATestosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Onl…D-0611-2017
March 8, 2017FDAAlfuzosin Hydrochloride Extended-release Tablets, 10 mg, 100-count bottles, Rx only, Dist…D-0502-2017
February 8, 2017FDASun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a) 100-count bottles (NDC 6275…D-0455-2017
February 1, 2017FDAbuPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, a) 60 (NDC 47335-737-…D-0445-2017
February 1, 2017FDAbuPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, 60 count bottles, Rx …D-0446-2017
November 30, 2016FDAKENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g…D-0148-2017
October 12, 2016FDAbuPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, Twice-A-Day, in 60 co…D-0007-2017
September 28, 2016FDACarvediol Tablets, USP, 6.25 mg, 100-count bottle (NDC 57664-244-18), 500-count bottle (N…D-1505-2016
September 28, 2016FDACarvediol Tablets, USP, 12.5 mg, 500-count bottle (NDC 57664-245-13), 1000-count bottle …D-1506-2016
September 28, 2016FDACarvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle …D-1504-2016
July 27, 2016FDAbuPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Only 60 tablets Distr…D-1446-2016

Questions about this company

How many recalls does SUN PHARMACEUTICAL INDUSTRIES INC have?
Recalert has 126 U.S. recalls on record for SUN PHARMACEUTICAL INDUSTRIES INC, published between July 17, 2013 and August 26, 2026.
Which agencies have handled SUN PHARMACEUTICAL INDUSTRIES INC recalls?
SUN PHARMACEUTICAL INDUSTRIES INC appears as the recalling firm in recalls from: FDA (126).

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