Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Syeda (drospirenone and ethinyl estradiol) Recalled by Sandoz Incorporated Due to Tablet/Capsule Imprinted with Wrong ID; a portion of...
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 Sandoz Incorporated directly.
Affected Products
Syeda (drospirenone and ethinyl estradiol), 3 mg/0.03 mg, 3 x 28 tablet blistercards, combination oral contraceptive tablet, Manufactured by Laboratorios Leon Farma S.A., Spain for Sandoz Inc., Princeton, NJ
Quantity: 17,188 cartons containing 3 cards each.
Why Was This Recalled?
Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could contain the incorrect debossing on one side of the tablet U2 instead of U3.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sandoz Incorporated
Sandoz Incorporated has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report