How many FDA warning letters has Teva Pharmaceuticals USA, Inc received?

Argus HQ has not recorded an FDA warning letter for Teva Pharmaceuticals USA, Inc in our current dataset.

What FDA recalls has Teva Pharmaceuticals USA, Inc issued?

Argus HQ has recorded 7 FDA recalls tied to Teva Pharmaceuticals USA, Inc.

Is Teva Pharmaceuticals USA, Inc FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 7 recalls, and 2 approval records for Teva Pharmaceuticals USA, Inc. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Teva Pharmaceuticals USA, Inc

Name: FDA Enforcement Actions Against Teva Pharmaceuticals USA, Inc
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_approval · anda2026-06-26
TEVA PHARMS INC — ANDA approval: NILOTINIB HYDROCHLORIDE (unspecified)
fda_approval · anda2026-06-22
TEVA PHARMS INC — ANDA approval: LO JUNEL FE (unspecified)
fda_recall · drug_recall2026-05-13
Teva Pharmaceuticals USA, Inc — Class II recall: Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30…
fda_recall · drug_recall2026-04-29
Teva Pharmaceuticals USA, Inc — Class II recall: Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, ND…
fda_recall · drug_recall2026-04-15
Teva Pharmaceuticals USA, Inc — Class II recall: Clonidine Transdermal System, USP, 0.3 mg/day, supplied in cartons of 4 Systems…
fda_recall · drug_recall2026-04-15
Teva Pharmaceuticals USA, Inc — Class II recall: Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems…
fda_recall · drug_recall2026-04-15
Teva Pharmaceuticals USA, Inc — Class II recall: Isotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufact…
fda_recall · drug_recall2026-04-15
Teva Pharmaceuticals USA, Inc — Class II recall: Clonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems…
fda_recall · drug_recall2026-04-15
Teva Pharmaceuticals USA, Inc — Class II recall: Isotretinoin Capsules, USP, 30 mg, Rx Only, 10 count Prescription Pack, Manufact…

Frequently asked questions

How many FDA warning letters has Teva Pharmaceuticals USA, Inc received?: Argus HQ has not recorded an FDA warning letter for Teva Pharmaceuticals USA, Inc in our current dataset.
What FDA recalls has Teva Pharmaceuticals USA, Inc issued?: Argus HQ has recorded 7 FDA recalls tied to Teva Pharmaceuticals USA, Inc.
Is Teva Pharmaceuticals USA, Inc FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 7 recalls, and 2 approval records for Teva Pharmaceuticals USA, Inc. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.