Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva Pharmaceuticals USA Due to Failed Impurities/Degradation Specifications: out of specification test results...
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 directly.
Affected Products
Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960.
Quantity: 17,473 cartons
Why Was This Recalled?
Failed Impurities/Degradation Specifications: out of specification test results for the norethindrone impurity.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report