FDANovember 24, 2025drug

Duloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactured by: Towa Pharmaceuticals Europe, S.L. Marotrelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceutical Inc., Berkeley Heights, NJ 07922 NDC 51991-748-10.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

What to do

FDA enforcement status: Ongoing

Brands named

breckenridge pharmaceuticalbreckenridge

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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