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Source: FDA | Recall date: 05/13/2026
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Affected product: Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle
Summary: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
Hazard: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
Track your baby products and get automatic recall alerts when something may affect your family.
Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.