Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by Teva Pharmaceuticals USA Due to CGMP deviations: Product bottle may be absent 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 Teva Pharmaceuticals USA directly.
Affected Products
Methylphenidate hydrochloride Extended-Release ablets USP (CII), 27 mg, 100-count bottle, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 62037-734-01
Quantity: 17,436 bottles
Why Was This Recalled?
CGMP deviations: Product bottle may be absent of desiccant.
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