Recalls / Class II
Class IID-0299-2026
Product
methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977. NDC 59762-4440-2
- Brand name
- Methylprednisolone
- Generic name
- Methylprednisolone
- Active ingredient
- Methylprednisolone
- Route
- Oral
- NDCs
- 59762-0049, 59762-4440, 59762-0050, 59762-0051
- FDA application
- NDA011153
- Affected lot / code info
- Lot # LG7675, Exp. Date Nov 2026
Why it was recalled
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.
Recalling firm
- Firm
- Greenstone Llc
- Manufacturer
- Mylan Pharmaceuticals Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 100 Route 206 North, N/A, Peapack, New Jersey 07977
Distribution
- Quantity
- 3456 cartons
- Distribution pattern
- Nationwide within the United States
Timeline
- Recall initiated
- 2026-01-15
- FDA classified
- 2026-01-28
- Posted by FDA
- 2026-02-04
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0299-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.