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Class II · ModerateActive recall

Methylprednisolone

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # LG7675, Exp. Date Nov 2026
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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 to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMylan Pharmaceuticals Inc.
Brand nameMETHYLPREDNISOLONE
Generic nameMETHYLPREDNISOLONE
Active ingredient(s)METHYLPREDNISOLONE
Distributed by / forGreenstone LLC, Peapack, NJ 07977
NDC59762-4440-2
Show the full FDA record
Full product labelmethylprednisolone 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
Recalling firmGreenstone Llc
DistributionNationwide within the United States
Quantity3456 cartons
Recall initiated2026-01-15
Report date2026-02-04
Recall completed—
Recall numberD-0299-2026
ClassificationClass II
FDA statusOngoing
Origin on filePeapack NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.