RecallRadar

FDA Drug recall D-1324-2014

BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 2 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093…

On 2014-05-28 the FDA classified a Class II recall of BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 2 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093… by Teva Pharmaceuticals Usa, citing failed Impurities/Degradation Specifications: High out of specification impurity test results were obtained during stability testing.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1324-2014
ClassificationClass II
Statusterminated
Initiated2014-04-07
Published2014-05-28
Last updated2026-09-13 11:51 UTC
CompanyTeva Pharmaceuticals Usa
DistributionUS

Product

BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets, 2 mg, 30-count bottles, Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-5378-56, UPC 3 0093-5378-56 5.

Reason

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

Identifiers

upc300935378565
code_infoLot #: 34013132A, 34013133A, 34013134A, 34013135A, 34013136A, Exp 11/14

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1324-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.