Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zeosa (norethindrone and ethinyl estradiol tablets USP Recalled by Teva Pharmaceuticals USA, Inc. Due to Impurities/Degradation: This recall is being carried out due...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA, Inc. directly.
Affected Products
Zeosa (norethindrone and ethinyl estradiol tablets USP, (chewable), 0.4 mg/0.035 mg, and ferrous fumarate tablets USP, (chewable) 75 mg), 3 Blister Cards, 28 Tablets Each, Rx only, TEVA Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-2090-28 and 0093-2090-58, cartons containing three (3) individual blister packs
Quantity: 100,761 cartons
Why Was This Recalled?
Impurities/Degradation: This recall is being carried out due to the potential for some lots not meeting impurity specifications.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA, Inc.
Teva Pharmaceuticals USA, Inc. has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report