Venlafaxine ER 150mg — Class III drug recall D-051-2013
Terminated recall by Stat Rx USA, reported 2012-11-21, distributed in GA, TN. Labeling: Label Mix-up: Product was incorrectly labeled,"Tabs" instead of "Capsules."
| Recall number | D-051-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stat Rx USA, Gainesville, GA, United States |
| Recall initiated | 2012-08-23 |
| Classified | 2012-11-09 |
| Reported by FDA | 2012-11-21 |
| Terminated | 2013-01-31 |
| Distributed | GA, TN |
| Quantity | 5 bottles |
| Reason classes | labeling |
| NDC | 42549-0684-30 |
| Lot numbers | 01/14, A00984 |
Product
Venlafaxine ER 150mg, 30 Tabs bottle, Generic for: Effexor, Packaged and Distributed by: Stat Rx USA, LLC, Gainesville, GA 30501 NDC 42549-684-30
Reason for recall
Labeling: Label Mix-up: Product was incorrectly labeled,"Tabs" instead of "Capsules."
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-051-2013. 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.