Drug FDA Class II Ongoing Mislabeling

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

Greenstone Llc Published Feb 4, 2026

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 60/100

What should you do?

Check whether you have this product, using the lot codes, UPCs, and dates listed below.
Do not eat, serve, or sell the affected product.
Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
Contact Greenstone Llc or your place of purchase with questions, and see the source record below for full details.

Reason for recall

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.

Affected products (1)

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

METHYLPREDNISOLONE · 3456 cartons

NDC: 59762-0049, 59762-4440, 59762-0050, 59762-0051, 59762-4440-3, 59762-4440-2, 59762-0049-1, 59762-0050-1, 59762-0051-1

Lot codes: LG7675

Code info: Lot # LG7675, Exp. Date Nov 2026

Affected areas

Nationwide

Timeline

Initiated

Jan 15, 2026
Published

Feb 4, 2026

Recall number: D-0299-2026
Agency: U.S. Food and Drug Administration
Country: US

Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.