Omeprazole Delayed Release Capsules — Class II drug recall D-0312-2021
Terminated recall by Golden State Medical Supply Inc., reported 2021-03-31, distributed in PA, TX. Failed Impurities/Degradation Specifications: Out of Specification results obtained for unknown impurities dur
| Recall number | D-0312-2021 |
|---|---|
| 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 | 2021-03-19 |
| Classified | 2021-03-24 |
| Reported by FDA | 2021-03-31 |
| Terminated | 2021-07-28 |
| Distributed | PA, TX |
| Reason classes | specification failure |
| NDC | 51407-0129-10 |
| Lot numbers | GS029673 |
| Expiration dates | 2021-05 |
Product
Omeprazole Delayed Release Capsules, USP, 20 mg, 1000-count bottles, Rx only, Packaged by GSMS Incorporated, Camarillo, CA 93012-8601 USA, NDC 51407-129-10
Reason for recall
Failed Impurities/Degradation Specifications: Out of Specification results obtained for unknown impurities during stability testing by manufacturer
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-0312-2021. 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.