Teva Pharmaceuticals USA recalls

Teva Pharmaceuticals USA has 281 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 21 Oct 2026. 52 are still ongoing. 21 were reported in the last 12 months. The most frequent reason is potency & assay.

Total recalls281since 2012
Last 12 months21reported
Class I62% of total
Ongoing52latest 21 Oct 2026

Recalls per month, last 24 months

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Severity split

Class I 6 2%Class II 210 75%Class III 65 23%

By year

Ongoing teva pharmaceuticals usa recalls

52 active

All teva pharmaceuticals usa recalls, newest first

281 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIMetoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets recalledMetoclopramideTeva Pharmaceuticals USAOtherNationwide
DrugCLASS IItraZODone Hydrochloride Tablets, USP, 50 mg recalledTrazodone HydrochlorideTeva Pharmaceuticals USAOtherNationwide
DrugCLASS IIOctreotide Acetate for Injectable Suspension recalledOctreotide AcetateTeva Pharmaceuticals USASterilityNationwide
DrugCLASS IIClaravis (isotretinoin capsule, USP), 10 mg, Packaged as a) recalledClaravisTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIIsotretinoin Capsules, USP, 30 mg recalled by Teva Pharmaceuticals USAIsotretinoinTeva Pharmaceuticals USAPotency & Assay4 states
DrugCLASS IIIsotretinoin Capsules, USP, 40 mg Prescription Pacs recalledIsotretinoinTeva Pharmaceuticals USAPotency & Assay4 states
DrugCLASS IIClonidine Transdermal System, USP, 0.3 mg/day, supplied recalledClonidine Transdermal SystemTeva Pharmaceuticals USAManufacturing (CGMP) DeviationsNJ
DrugCLASS IIClonidine Transdermal System, USP, 0.1 mg/day, supplied recalledClonidine Transdermal SystemTeva Pharmaceuticals USAManufacturing (CGMP) DeviationsNJ
DrugCLASS IIClonidine Transdermal System, USP, 0.2 mg/day, supplied recalledClonidine Transdermal SystemTeva Pharmaceuticals USAManufacturing (CGMP) DeviationsNJ
DrugCLASS IIOctreotide Acetate for Injectable Suspension recalledOctreotide AcetateTeva Pharmaceuticals USASterilityNationwide
DrugCLASS IIOctreotide Acetate for Injectable Suspension recalledOctreotide AcetateTeva Pharmaceuticals USASterilityNationwide
DrugCLASS IIOctreotide Acetate for Injectable Suspension recalledOctreotide AcetateTeva Pharmaceuticals USASterilityNationwide
DrugCLASS IIMetoprolol Succinate Extended-Release Tablets recalledMetoprolol SuccinateTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIMetoprolol Succinate Extended-Release Tablets, 200 mg recalledMetoprolol SuccinateTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIMetoprolol Succinate Extended-Release Tablets, 25 mg bottles recalledMetoprolol SuccinateTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIMetoprolol Succinate Extended-Release Tablets, 50 mg bottles recalledMetoprolol SuccinateTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIICarton label: Testosterone Gel 1% per unit dose, Ciii-dose packets recalledTestosteroneTeva Pharmaceuticals USAPackaging DefectsNationwide
DrugCLASS IIAmoxicillin and Clavulanate Potassium recalledTeva Pharmaceuticals USAPotency & AssayCA, MS, OH
DrugCLASS IIPrazosin Hydrochloride, Capsules, USP, 5 mg recalledTeva Pharmaceuticals USANitrosamine ImpurityNationwide
DrugCLASS IIPrazosin Hydrochloride, Capsules, USP, 1 mg recalledTeva Pharmaceuticals USANitrosamine ImpurityNationwide
DrugCLASS IIPrazosin Hydrochloride, Capsules, USP, 2 mg recalledTeva Pharmaceuticals USANitrosamine ImpurityNationwide
DrugCLASS IIMetoclopramide Tablets, USP 10 mg recalled by Teva Pharmaceuticals USAMetoclopramideTeva Pharmaceuticals USAOtherNationwide
DrugCLASS IIGranix (tbo-filgrastim) Injection 300 mcg recalledTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IITestosterone Gel, 1.62%, (Alcohol 80% v/v)-dose packets recalledTestosteroneTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIFludrocortisone Acetate Tablets, USP 0.1mg recalledTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIAmoxicillin and Clavulanate Potassium Tablets recalledTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIIsotretinoin Capsules, USP 40mg blister packs recalledIsotretinoinTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IITri-Lo-Sprintec (norgestimate recalled by Teva Pharmaceuticals USATri-lo-sprintecTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIINortrel 7/7/7 (norethindrone recalled by Teva Pharmaceuticals USANortrel 7/7/7Teva Pharmaceuticals USAPackaging DefectsNationwide
DrugCLASS IIINortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35 recalledNortrelTeva Pharmaceuticals USAPackaging DefectsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.