Glimepiride Tablets — Class II drug recall D-0552-2023
Ongoing recall by Northwind Pharmaceuticals LLC, reported 2023-05-03, distributed nationwide. CGMP Deviations
| Recall number | D-0552-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Northwind Pharmaceuticals LLC, Indianapolis, IN, United States |
| Recall initiated | 2023-03-16 |
| Classified | 2023-04-26 |
| Reported by FDA | 2023-05-03 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| NDC | 51655-0120, 51655-0120-26, 51655-0120-52 |
| Lot numbers | F105692201, F105692202, F105692203 |
| Expiration dates | 2024-09-30, 2025-02-28 |
Product
Glimepiride Tablets, USP 4mg, packaged in a) 30-count bottles (NDC 51655-120-52), and b) 90-count bottles (NDC 51655-120-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.
Reason for recall
CGMP Deviations
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-0552-2023. 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.