Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35 Recalled by Teva Pharmaceuticals USA, Inc Due to Discoloration: discolored tablets (shades of blue) mixed in...
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
Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9008-67
Quantity: 12,916 cartons
Why Was This Recalled?
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA, Inc
Teva Pharmaceuticals USA, Inc has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report