US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Apr 30, 2026 (4 months ago)

Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in…

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

Why it was recalled

Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.

What was recalled

Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by: Safecor, Columbus, OH 43204. NDC: 64380-474-01

Recalling firm
Safecor Health, LLC
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0538-2026

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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