Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets Recalled by Watson Laboratories Inc Due to Failed Tablet/Capsule Specification; tablet breakage while pushing through...
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 Watson Laboratories Inc directly.
Affected Products
ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets, 3.0 mg/0.03 mg, Rx only, 3 tablet dispensers, 28 tablets each, Manuf. by: Watson Laboratories, Inc., Corona, CA 92880. USA; Distributed by: Watson Pharma, Inc., Corona, CA 92880 USA. NDC 52544-981-31 Carton; NDC 52544-981-28
Quantity: 136,720 cartons
Why Was This Recalled?
Failed Tablet/Capsule Specification; tablet breakage while pushing through the blister pack (dispenser) .
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Watson Laboratories Inc
Watson Laboratories Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report