Greenstone LLC recalled 3,456 cartons of methylprednisolone tablets on January 15, 2026. The recall follows reports of incorrect dosing information due to misapplied blister foil. Consumers should stop using the product immediately and contact their healthcare provider.
Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.
Consumers and healthcare providers should stop using this product immediately. Contact Greenstone Llc or your healthcare provider for guidance. Notification method: Letter
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Methylprednisolone tablets are corticosteroids used to treat a variety of conditions such as inflammation, allergies, and autoimmune disorders. Patients typically receive these medications through a prescription from healthcare providers.
The hazard arises from the incorrect orientation of the blister foil, which misleads users about the correct dosage. This can lead to patients taking more or less medication than prescribed, impacting their treatment.
This recall is not part of a broader industry pattern.
Consumers may face health risks if they continue using the affected product. The recall requires immediate action to prevent potential health issues linked to incorrect dosage.
The lot number and expiration date are typically located on the back or bottom of the blister card packaging.
Expect a refund processing time of approximately 4-6 weeks after returning the product.
Keep a record of any correspondence with the manufacturer and retain receipts or documentation regarding the purchase.
This recall affects methylprednisolone tablets, USP Dosepak, 4 mg, distributed by Greenstone LLC. The product comes in a carton containing 21 tablets and has an NDC of 59762-4440-2. The affected lot number is LG7675, with an expiration date of November 2026.
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