Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Gildess 24 FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical, Inc. Due to Subpotent Drug; Ethinyl Estradiol
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 Par Pharmaceutical, Inc. directly.
Affected Products
Gildess 24 FE 1.5/30 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, (a) 3 blisters (NDC 0603-7610-49), and (b) 6 blisters (NDC 0603-7610-17), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST PHARMACEUTICALS, USA, Huntsville, AL 35811
Quantity: 44,127 tablets
Why Was This Recalled?
Subpotent Drug; Ethinyl Estradiol
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Par Pharmaceutical, Inc.
Par Pharmaceutical, Inc. has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report