Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva Pharmaceuticals USA Due to Failed Impurities/Degradation Specifications: High out of specification impurity...
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
BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 8 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-5379-56, UPC 3 0093-5379-56 2.
Quantity: 53,452 bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications: High out of specification impurity test results were obtained during stability testing.
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