Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Paliperidone Extended Release Tablets 9 mg Recalled by Teva Pharmaceuticals USA Due to Defective Delivery System: There is a potential for...
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
Paliperidone Extended Release Tablets 9 mg, packaged in a) 30-count bottle(NDC 0591-3695-30) , b) 90-count bottle (NDC 0591-3695-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054
Quantity: 3,785 bottles
Why Was This Recalled?
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Where Was This Sold?
This product was distributed to 1 state: IL
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