--- title: "Teva Pharmaceuticals USA Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Teva Pharmaceuticals USA recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/teva-pharmaceuticals-usa/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Teva Pharmaceuticals USA recall records **0** reported ongoing 10 records in this archive. Latest source date Jan 18, 2022. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jan 18, 2022 FDA drug enforcement ### [Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale...](https://isitonrecall.com/recall/fda-drug-d-0461-2022-doxylamine-succinate-and-pyridoxine-hydrochloride-delayed-release-tablets-10-mg-10-mg-100-count-bott/) Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient Class II Reported terminated Distribution: Nationwide in the USA [Official source for Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0461-2022%22) Jan 10, 2022 FDA drug enforcement ### [Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-0808-02](https://isitonrecall.com/recall/fda-drug-d-0520-2022-tretinoin-capsules-10-mg-100-count-bottle-rx-only-teva-pharmaceuticals-usa-inc-north-wales-pa-19454/) Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution. Class II Reported terminated Distribution: nationwide in the USA [Official source for Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0520-2022%22) Jan 7, 2022 FDA drug enforcement ### [Mimvey (estradiol and norethindrone acetate tablets USP), 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Ma...](https://isitonrecall.com/recall/fda-drug-d-0521-2022-mimvey-estradiol-and-norethindrone-acetate-tablets-usp-1-mg-0-5-mg-packaged-in-cartons-of-28-tablets/) Mislabeling Class III Reported terminated Distribution: USA Nationwide [Official source for Mimvey (estradiol and norethindrone acetate tablets USP), 1 mg/0.5 mg, packaged in cartons of 28 ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0521-2022%22) Jan 7, 2022 FDA drug enforcement ### [Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx Only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Man...](https://isitonrecall.com/recall/fda-drug-d-0522-2022-mimvey-estradiol-and-norethindrone-acetate-tablets-usp-1-mg-0-5-mg-packaged-in-cartons-of-28-tablets/) Mislabeling Class III Reported terminated Distribution: USA Nationwide [Official source for Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg, packaged in cartons of 28 T...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0522-2022%22) Dec 31, 2021 FDA drug enforcement ### [MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufacture...](https://isitonrecall.com/recall/fda-drug-d-0370-2022-methylprednisolone-acetate-injectable-suspension-usp-400-mg-10ml-40mg-ml-10-ml-multiple-dose-vial-rx/) Lack of Assurance of Sterility Class II Reported terminated Distribution: Methylprednisolone, TN Norepinephrine BItartrate - MS, OH [Official source for MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose V...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0370-2022%22) Dec 31, 2021 FDA drug enforcement ### [Norepinephrine Bitartrate Injection USP 4 mg/4 mL (1 mg/mL), 4 mL Single-Dose Vials, 10 vials per carton, Rx Only, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, N...](https://isitonrecall.com/recall/fda-drug-d-0371-2022-norepinephrine-bitartrate-injection-usp-4-mg-4-ml-1-mg-ml-4-ml-single-dose-vials-10-vials-per-carton/) Lack of Assurance of Sterility Class II Reported terminated Distribution: Methylprednisolone, TN Norepinephrine BItartrate - MS, OH [Official source for Norepinephrine Bitartrate Injection USP 4 mg/4 mL (1 mg/mL), 4 mL Single-Dose Vials, 10 vials per...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0371-2022%22) Dec 16, 2021 FDA drug enforcement ### [Penicillin V Potassium for Oral Solution, USP 125 mg (200,000 U) per 5 mL a) 100 mL (NDC 00093-4125-73) and b) 200 mL (NDC 00093-4125-74) (when mixed) bottles, Rx Only, Manufact...](https://isitonrecall.com/recall/fda-drug-d-0294-2022-penicillin-v-potassium-for-oral-solution-usp-125-mg-200-000-u-per-5-ml-a-100-ml-ndc-00093-4125-73-an/) Subpotent Class II Reported terminated Distribution: nationwide [Official source for Penicillin V Potassium for Oral Solution, USP 125 mg (200,000 U) per 5 mL a) 100 mL (NDC 00093-41...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0294-2022%22) Dec 8, 2021 FDA drug enforcement ### [Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml dropper bottles (NDC 0591-2127-79), and b) 15 ml dropper bottles (NDC 0591-2127-12), Rx Only, Manufactured in Ind...](https://isitonrecall.com/recall/fda-drug-d-0373-2022-brinzolamide-ophthalmic-suspension-usp-1-packaged-as-a-10-ml-dropper-bottles-ndc-0591-2127-79-and-b/) Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing. Class II Reported terminated Distribution: Nationwide in the USA [Official source for Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml dropper bottles (NDC 0591-2127-79...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0373-2022%22) Oct 28, 2021 FDA drug enforcement ### [Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake City, UT, Distributed by: Actavis Pharma, ...](https://isitonrecall.com/recall/fda-drug-d-0235-2022-clonidine-transdermal-system-usp-0-1-mg-day-4-patches-per-carton-rx-only-manufactured-by-actavis-lab/) Failed Impurities/Degradation Specifications Class III Reported terminated Distribution: Nationwide and Puerto Rico [Official source for Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Act...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0235-2022%22) Oct 27, 2021 FDA drug enforcement ### [Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg, Rx Only, 90 capsules, labelled as (a) Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ ...](https://isitonrecall.com/recall/fda-drug-d-0232-2022-cartia-xt-diltiazem-hydrochloride-extended-release-capsules-usp-120-mg-rx-only-90-capsules-labelled/) Labelling: Incorrect Exp. Date Class II Reported terminated Distribution: Distributed Nationwide in the USA [Official source for Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg, Rx Only, 90 capsules, ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0232-2022%22) ## Reasons in these listed records - Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient - Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution. - Mislabeling - Lack of Assurance of Sterility These examples come from this result page and are not a ranking of every recall reason. ## Checking Teva Pharmaceuticals USA ### Is there a recall on teva pharmaceuticals usa right now? This archive contains 10 records, including 0 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Teva Pharmaceuticals USA](https://isitonrecall.com/check/?q=Teva%20Pharmaceuticals%20USA) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)