US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 7, 2014 (12 years ago)

BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 8 mg, 30-count bottles, Rx only, Teva…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Impurities/Degradation Specifications: High out of specification impurity test results were obtained during stability testing.

What was recalled

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.

Recalling firm
Teva Pharmaceuticals USA
NDC code
0093-5379-56
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1325-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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