Teva Pharmaceuticals USA: 164 recalls on record

Recalls filed with 1 agency: FDA (164).

First recall on record: November 27, 2013. Most recent: February 9, 2022.

Risk classification: Class I: 2 · Class II: 128 · Class III: 34

Most recent recalls

DateAgencyProduct
December 19, 2018FDAAmlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/320 mg/25 mg, (a) 30-count …D-0310-2019
December 19, 2018FDAAmlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles (NDC 0093-7693-56) & …D-0306-2019
December 19, 2018FDAAmlodipine and Valsartan Tablets 10 mg/160 mg, (a) 30-count bottles (NDC 0093-7961-56) & …D-0304-2019
December 19, 2018FDAAmlodipine and Valsartan Tablets 5 mg/320 mg, (a) 30-count bottles (NDC 0093-7692-56) & 9…D-0305-2019
December 19, 2018FDAAmlodipine and Valsartan Tablets 5 mg/160 mg, (a) 30-count bottles (NDC 0093-7690-56) & 9…D-0303-2019
October 31, 2018FDAMetoprolol Succinate Extended Release Tablets, USP 50 mg, 100-count bottle, Rx only, Manu…D-0129-2019
October 31, 2018FDAPaliperidone Extended Release Tablets 9 mg, packaged in a) 30-count bottle(NDC 0591-3695-…D-0097-2019
October 31, 2018FDAPaliperidone Extended Release Tablets 3 mg, packaged in a) 30-count bottle(NDC 0591-3693-…D-0096-2019
October 31, 2018FDAMetformin Hydrochloride Extended Release Tablets, 500 mg, 100-count bottle, Rx only, Manu…D-0099-2019
August 15, 2018FDAOmega-3-Acid Ethyl Esters Capsules USP, 1 gram* 120-count bottle Rx Only. Manufactured b…D-1074-2018
August 1, 2018FDAValsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 80 mg/12.5 mg tablets, 90 count-cou…D-0981-2018
August 1, 2018FDAValsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/25 mg tablets, USP 90-count …D-0983-2018
August 1, 2018FDAValsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/12.5 mg tablets, USP 90-coun…D-0982-2018
August 1, 2018FDAValsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/12.5 mg tablets, USP, 90-cou…D-0984-2018
August 1, 2018FDAValsartan Tablets, USP 80 mg, 90-count bottle (NDC 0591-2168-19), 1000-count bottle (NDC …D-0987-2018
August 1, 2018FDAValsartan Tablets, USP 160 mg, 90-count bottle (NDC 0591-2169-19), 1000-count bottle (NDC…D-0988-2018
August 1, 2018FDAValsartan Tablets, USP 40 mg, 30-count bottle (NDC 0591-2167-30), 90-count bottle (NDC 05…D-0986-2018
August 1, 2018FDAValsartan Tablets, USP 320 mg, 90-count bottle (NDC 0591-2170-19), 500-count bottle (NDC …D-0989-2018
May 30, 2018FDALidocaine Patch 5% (700 mg) ,(NDC 0591-3525-11), 30 envelopes containing 1 patch each/ 30…D-0857-2018
March 28, 2018FDAEstradiol Vaginal Inserts, USP 10 mcg, packaged in a) 8 inserts/carton (NDC 0093-3223-08)…D-0620-2018
February 21, 2018FDAFluoxetine Tablets USP, 10 mg, 30-count bottle, Rx only, Manufactured in Israel by: Teva …D-0578-2018
February 14, 2018FDAFentanyl Transdermal System. 25 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3198-…D-0540-2018
February 14, 2018FDAFentanyl Transdermal System, 50 mcg/h, packaged in 5 pouch system cartons (NDC 0591-3212-…D-0541-2018
February 14, 2018FDAFentanyl Transdermal System, 100 mcg/h, packaged in 5 pouch system (NDC 0591-3214-72), R…D-0543-2018
January 17, 2018FDAMoexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count b…D-0208-2018

Questions about this company

How many recalls does Teva Pharmaceuticals USA have?
Recalert has 164 U.S. recalls on record for Teva Pharmaceuticals USA, published between November 27, 2013 and February 9, 2022.
Which agencies have handled Teva Pharmaceuticals USA recalls?
Teva Pharmaceuticals USA appears as the recalling firm in recalls from: FDA (164).

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