FDA recall record

Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in recall — FDA D-0538-2026

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

Class IIclassification
D-0538-2026official record ID
May 27, 2026report date

Recall record at a glance

Official recordD-0538-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSafecor Health, LLC
Report dateMay 27, 2026
Recall initiation dateApr 30, 2026
Quantity149 capsules
LocationColumbus, OH, United States

Official product description

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

Why the product was recalled

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

Distribution information

TX only

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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