Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by:
Manufacturer / Brand: Safecor Health, LLC
Reason for Recall
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
Date Issued
Category
Medications
Status
unknown
About Medications recalls
Drug recalls in the United States are overseen by the FDA's Center for Drug Evaluation and Research. They may be initiated voluntarily by the manufacturer or requested by the FDA when contamination, potency issues, or labeling errors are identified. Class I drug recalls — the most serious — involve situations where the product may cause serious injury or death. Before stopping a prescription medication due to a recall, contact your pharmacist or prescriber: for many medications, abrupt discontinuation carries its own risks. Your pharmacy can usually arrange an emergency replacement from an unaffected lot or an alternative manufacturer at no additional cost.
What to do if you're affected
- →Stop taking the medication if it matches the recalled lot number.
- →Contact your doctor or pharmacist before stopping any prescription.
- →Return the product to your pharmacy for a refund or replacement.
- →Call the manufacturer's hotline listed on the official recall notice.
About mislabeling recalls
Mislabeling recalls occur when a product's packaging contains incorrect information — wrong ingredients, inaccurate net weight, incorrect usage instructions, or packaging mix-ups where the wrong product ends up in a container. While many mislabeling issues are low-risk, they can be dangerous when the label omits allergens, provides incorrect dosing information for a medication, or creates confusion about a product's contents.
⚠ Check any remaining product carefully against the official recall notice to confirm whether your specific lot or batch is affected.
Opens the official government source. Always refer to official sources for the most current information.