Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
risperiDONE ORALLY DISINTEGRATING TABLETS Recalled by Zydus Pharmaceuticals USA Inc Due to Failed Impurities/Degradation Specifications: Out of specification for a...
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 Zydus Pharmaceuticals USA Inc directly.
Affected Products
risperiDONE ORALLY DISINTEGRATING TABLETS, 2 mg, 30 Ct Bottles, Rx Only. Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC: 68382-156-06.
Quantity: 9504 Bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications: Out of specification for a known degradant.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zydus Pharmaceuticals USA Inc
Zydus Pharmaceuticals USA Inc has 41 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report