Venlafaxine Hydrochloride Extended-Release Capsules — Class II drug recall D-1458-2016
Terminated recall by Golden State Medical Supply Inc., reported 2016-08-24, distributed nationwide. Failed Dissolution Specifications: Out-of-specification results in retained sample.
| Recall number | D-1458-2016 |
|---|---|
| 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 | 2016-08-03 |
| Classified | 2016-08-16 |
| Reported by FDA | 2016-08-24 |
| Terminated | 2017-02-02 |
| Distributed | Nationwide (US) |
| Quantity | 65,401 bottles |
| Reason classes | specification failure |
| NDC | 60429-0123-30, 60429-0123-90 |
| Expiration dates | 2017-10, 2017-11 |
Product
Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.
Reason for recall
Failed Dissolution Specifications: Out-of-specification results in retained sample.
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-1458-2016. 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.