Ezetimibe and Simvastatin Tablets — Class II drug recall D-0227-2022
Terminated recall by Golden State Medical Supply Inc., reported 2021-11-17, distributed in AZ, MO. Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipi
| Recall number | D-0227-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Golden State Medical Supply Inc., Camarillo, CA, United States |
| Recall initiated | 2021-10-14 |
| Classified | 2021-11-09 |
| Reported by FDA | 2021-11-17 |
| Terminated | 2022-11-10 |
| Distributed | AZ, MO |
| Reason classes | specification failure |
| NDC | 51407-0190, 51407-0190-10, 51407-0190-30, 51407-0190-90, 51407-0191, 51407-0191-10, 51407-0191-30, 51407-0191-90, 51407-0192, 51407-0192-05, 51407-0192-10, 51407-0192-30, 51407-0192-90, 51407-0193, 51407-0193-05, 51407-0193-30, 51407-0193-90 |
| Lot numbers | GS038610 |
| Expiration dates | 2023-01 |
Product
Ezetimibe and Simvastatin Tablets, 10 mg/40mg, a) 90 Tablets, b) 500 tablets, Rx only, Manufactured by Dr. Reddy's Laboratories LA LLC Shreveport, LA 71106 USA, Packaged by GSMS, Incorporated Camarillo, CA 93012 USA; NDC: a) 51407-192-90, b) 51407-192-05
Reason for recall
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle
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-0227-2022. 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.