Drug recall
Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b)…
FDA recall event 74847 · Class II · Golden State Medical Supply Inc.
Key facts
| Event ID | 74847 |
|---|---|
| Recall numbers | D-1458-2016, D-1459-2016 |
| Recalling firm | Golden State Medical Supply Inc. |
| Product type | Drugs |
| Products | 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., Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specifications: Out-of-specification results in retained sample. |
| Initiation date | Aug 3, 2016 |
| Report date | Aug 24, 2016 |
| Termination date | Feb 2, 2017 |
| City | Camarillo |
| State | CA |
| Country | United States |
| FEI number | 3006458969 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: