methylprednisolone tablets — Class II drug recall D-0299-2026
Ongoing recall by Greenstone Llc, reported 2026-02-04, distributed nationwide. Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities,
| Recall number | D-0299-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Greenstone Llc, Peapack, NJ, United States |
| Recall initiated | 2026-01-15 |
| Classified | 2026-01-28 |
| Reported by FDA | 2026-02-04 |
| Distributed | Nationwide (US) |
| Quantity | 3,456 cartons |
| Reason classes | labeling |
| NDC | 59762-0049, 59762-0049-01, 59762-0050, 59762-0050-01, 59762-0051, 59762-0051-01, 59762-4440, 59762-4440-02, 59762-4440-03 |
| Lot numbers | LG7675 |
| Expiration dates | 2026-11-20 |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0299-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.