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Recall Observatory FDA recall evidence

Drug product

Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA.

D-0069-2018

October 25, 2017

Class II

Product summary

Firm
Teva Pharmaceuticals USA
Event
Event 78364
Status
Terminated
Classification
Class II
Quantity
140,993 bottles
Official record key
drug-enforcement:D-0069-2018

Official wording

Reason: Failed dissolution specifications; all lots within expiry are being recalled due to out of specification dissolution results.

Code information: Lot Numbers: a) 1089376A, 1089382A, 1095210M, 1117768M, 1117769A, Exp. 11/17; 1128452A, 1128453A, 1137658A, 1154207A, 1156087A, Exp. 03/18; b) 1089379A, 1091533M, 1125206A, Exp. 11/17; 1128456A, 1147665A, 1154208A, 1156088A, Exp. 03/18.

Distribution pattern: Nationwide in the USA and Puerto Rico.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out of specification