Quick Facts at a Glance
- Recall Date
- January 15, 2026
- Hazard Level
- HIGH
- Brands
- METHYLPREDNISOLONE, Mylan Pharmaceuticals Inc.
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- METHYLPREDNISOLONE, Mylan Pharmaceuticals Inc.
- Product type
- Methylprednisolone Tablets
- Model numbers
- Lot # LG7675, Exp. Date Nov 2026
- UPC codes
- 59762-0049, 59762-4440, 59762-0050, 59762-0051, 59762-4440-3, 59762-4440-2, 59762-0049-1, 59762-0050-1 +1 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 15, 2026
Reported by FDA DRUG
February 4, 2026
RecallRadar source check
February 11, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Greenstone Llc or your healthcare provider for guidance. Notification method: Letter
About This Product
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.
Why This Is Dangerous
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.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
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.
Practical Guidance
How to identify if yours is affected
- Check the lot number on the blister card.
- Verify the expiration date is November 2026.
- If you have lot number LG7675, your product is affected.
Where to find product info
The lot number and expiration date are typically located on the back or bottom of the blister card packaging.
What timeline to expect
Expect a refund processing time of approximately 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all communication attempts with Greenstone LLC.
- Consider contacting the FDA for further assistance.
- Explore consumer protection agencies if further issues arise.
How to prevent similar issues
- Always check for recalls on medications before use.
- Be aware of labeling and dosage instructions on medication packaging.
- Consult with healthcare providers for any medication concerns.
Documentation advice
Keep a record of any correspondence with the manufacturer and retain receipts or documentation regarding the purchase.
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Product Details
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.
Key Facts
- Recall date: January 15, 2026
- Quantity recalled: 3,456 cartons
- Incorrect dosing information due to blister foil error
- Contact Greenstone LLC for refund process
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Safety Guide
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