Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Methylphenidate Hydrochloride Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed Dissolution Specifications: Low out of specification results...
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
Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 0591-5884-01.
Quantity: 58,292 bottles
Why Was This Recalled?
Failed Dissolution Specifications: Low out of specification results for dissolution.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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