Zydus Pharmaceuticals (USA) Inc: 85 recalls on record

Recalls filed with 1 agency: FDA (85).

First recall on record: August 8, 2012. Most recent: August 12, 2026.

Risk classification: Class I: 2 · Class II: 69 · Class III: 14

Most recent recalls

DateAgencyProduct
December 23, 2020FDALansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg, 100 Tablets (10 x 10 u…D-0146-2021
November 11, 2020FDALansoprazole Delayed-Release Orally Disintegrating Tablets 30 mg, 100-count carton (10 x1…D-0075-2021
November 11, 2020FDALansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg, 100-count carton (10 x1…D-0074-2021
February 19, 2020FDAEthacrynate Sodium for Injection, USP, 50mg/vial, Single Dose Vial, Rx Only, Manufactured…D-0834-2020
June 26, 2019FDAPramipexole Dihydrochoride Tablets 0.25 mg, 90-count bottle, Rx Only, Manufactured by: Ca…D-1444-2019
June 26, 2019FDAMethylPREDNISolone Tablets, USP 8 mg, 25 tablets, Rx Only, Manufactured by: Cadila Health…D-1453-2019
June 26, 2019FDAMethylPREDNISolone Tablets, USP 4 mg per tablet, 21 Tablets dosepack, Rx Only, Made in I…D-1449-2019
June 26, 2019FDAPramipexole Dihydrochloride Tablets 0.5 mg, 90-count bottle, Rx only, Manufactured by: Ca…D-1446-2019
June 26, 2019FDAAnastrozole Tablets, USP, 1 mg, 1,000-count bottle, Rx only, Manufactured by: Cadila Hea…D-1441-2019
June 26, 2019FDAMethylPREDNISolone Tablets, USP 16 mg, 50 tablets, Rx only, Manufactured by: Cadila Healt…D-1450-2019
June 26, 2019FDAMethylPREDNISolone Tablets, USP, 4 mg, 100 tablets, Rx only, Manufactured by: Cadila Heal…D-1448-2019
May 15, 2019FDAAcyclovir Tablets, USP, 400 mg, 100 count bottles, Rx Only Manufactured by: Cadila Health…D-1272-2019
December 6, 2017FDAParoxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-…D-0101-2018
September 20, 2017FDAParoxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthca…D-1137-2017
August 9, 2017FDADivalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufa…D-1041-2017
August 9, 2017FDADivalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-0…D-1043-2017
August 9, 2017FDADivalproex Sodium Delayed Release Tablets, USP, 250 mg 100-count bottle (NDC 68382-032-01…D-1042-2017
April 5, 2017FDADivalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) …D-0617-2017
March 29, 2017FDAATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) …D-0605-2017
December 28, 2016FDABuPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, Rx Only, a) 30 count bott…D-0207-2017
November 30, 2016FDABuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 300 mg, Rx Only, 500-count bo…D-0149-2017
September 14, 2016FDABromocriptine Mesylate Capsules USP, 5 mg, 30-count bottles, Rx only, Manufactured by: Ca…D-1491-2016
August 24, 2016FDAVenlafaxine HCL ER Capsule USP, 150mg, packaged in a) 30-count bottles (NDC 68382-036-06)…D-1460-2016
August 24, 2016FDAVenlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06),…D-1461-2016
March 2, 2016FDArisperiDONE ORALLY DISINTEGRATING TABLETS, 2 mg, 30 Ct Bottles, Rx Only. Manufactured by:…D-0725-2016

Questions about this company

How many recalls does Zydus Pharmaceuticals (USA) Inc have?
Recalert has 85 U.S. recalls on record for Zydus Pharmaceuticals (USA) Inc, published between August 8, 2012 and August 12, 2026.
Which agencies have handled Zydus Pharmaceuticals (USA) Inc recalls?
Zydus Pharmaceuticals (USA) Inc appears as the recalling firm in recalls from: FDA (85).

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