US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jan 15, 2026 (8 months ago)

methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

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.

What was recalled

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

Recalling firm
Greenstone Llc
NDC code
59762-4440-2
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0299-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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