Greenstone recalls methylprednisolone tablets due to incorrect dosing information on blister packaging. This may lead to improper medication doses if users follow the foil instructions.
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.
Greenstone is recalling methylprednisolone tablets that have incorrect dosing information on the blister packaging. If users follow the foil instructions, they might take the wrong dose of medication.
The blister foil is incorrectly oriented, so the dosing information on the foil does not match the actual tablet contents. This could lead to users taking the wrong dose if they follow the foil instructions.
People who have received the recalled methylprednisolone tablets from Greenstone LLC. Those who use the tablets as prescribed by a doctor are most at risk.
Check for the NDC code 59762-4440-2 on the packaging. The product was distributed by Greenstone LLC and contains 21 tablets per blister card.
Look for the NDC code 59762-4440-2 on the packaging to identify the recalled product.
The product is safe to use if the user follows the correct dosing instructions as provided by their doctor, but the packaging has incorrect dosing information that could lead to improper doses.
Check for the NDC code 59762-4440-2 on the packaging. The product contains 21 tablets per blister card and was distributed by Greenstone LLC.
The recall does not specify a remedy, so contact your doctor for guidance on whether to continue using the product.
We’ve drafted a message you can send Greenstone to request your refund or repair — edit it as you like.
Subject: Recall D-0299-2026 — Greenstone Greenstone Hello, I own a Greenstone that is covered by recall D-0299-2026 from Greenstone. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
