HIGH

Greenstone Recalls Methylprednisolone Tablets Due to Dosing Error

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.

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

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

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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.

The Hazard

The recall stems from incorrect orientation of the blister foil on the tablets. This misorientation leads to incorrect dosing information, posing a risk of improper medication administration.

What to Do

Stop using the affected methylprednisolone tablets immediately. Contact Greenstone LLC or your healthcare provider for further guidance and information on obtaining a refund.

Contact Information

For more information, consumers can visit the FDA recall page or call Greenstone LLC directly. Additionally, healthcare providers should advise patients accordingly.

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot # LG7675
Exp. Date Nov 2026
UPC Codes
59762-0049
59762-4440
59762-0050
+6 more
Affected States
ALL
Report Date
February 4, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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