Methylprednisolone Recall: Greenstone Dosepak 4 mg
Announced 2026-02-04 · FDA
FDA recalls Greenstone methylprednisolone tablets, USP Dosepak, 4 mg, 21 tablets per blister card, Rx only, distributed nationwide, due to incorrect blister foil orientation that may cause dosing information on the foil to be read incorrectly. The affected lot is LG7675 with expiration date November 2026.
| Brand | Greenstone Llc |
|---|---|
| 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 |
| Reason | 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. |
| Severity | moderate |
| Units affected | 3456 |
| Distribution | Nationwide within the United States |
| Agency | FDA |
| Recall / campaign no. | Lot # LG7675, Exp. Date Nov 2026 |
WHAT YOU SHOULD DO
- Do not use methylprednisolone Dosepak from lot LG7675 exp Nov 2026.
- Return the product to your pharmacy or follow recall instructions for disposal or replacement.
- If you have questions or have used the product, contact your healthcare provider or pharmacist.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.