Teva North America recalls

Teva North America has 12 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 12 Oct 2016. The most frequent reason is potency & assay.

Total recalls12since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 12 Oct 2016

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 8 67%Class III 4 33%

Why teva north america is recalled

Product types

Brands

By year

All teva north america recalls, newest first

12 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIClaravis (isotretinoin capsules USP), 10mg recalledTeva North AmericaPotency & AssayNationwide
DrugCLASS IIOndansetron Injection USP 40 mg/ (2 mg/mL) recalledTeva North AmericaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIEptifibatide Injection 75 mg/ 75 mg/mL) single use vial recalledTeva North AmericaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILinezolid Injection 600 mg recalled by Teva North AmericaTeva North AmericaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIArgatroban Injection in 9% Sodium Chloride 250 mg/ (1 mg/mL) recalledTeva North AmericaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIAmoxicillin for Oral Suspension USP, 400 mg recalledAmoxicillinTeva North AmericaPotency & AssayNationwide
DrugCLASS IIAlbuterol Sulfate Syrup, 2 mg recalled by Teva North AmericaTeva North AmericaParticulate MatterNationwide
DrugCLASS IIIChildren's Qnasl 40 mcg (beclomethasone dipropionate) Nasal recalledTeva North AmericaPotency & AssayNationwide
DrugCLASS IIImitoXANTRONE Injection USP (concentrate), 20 mg recalledTeva North AmericaPotency & AssayNationwide
DrugCLASS IIIDivalproex Sodium Delayed-release Tablets USP, RX, 250 mg recalledTeva North AmericaOtherNationwide

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.