Venlafaxine recalls

The FDA has published 26 recalls involving Venlafaxine since 2012. The latest was reported on 16 Apr 2025. Most were for potency & assay. Aidapak Services has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls26since 2012
Last 12 months0reported
Class I14% of total
Ongoing0latest 16 Apr 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 4%Class II 21 81%Class III 4 15%

By year

All venlafaxine recalls, newest first

26 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIVenlafaxine Tablets, USP, 75 mg recalled by Zydus Pharmaceuticals (USA)VenlafaxineZydus PharmaceuticalsForeign MaterialNationwide
DrugCLASS IIIVenlafaxine Extended-Release Tablets, 150mg recalled by Appco PharmaVenlafaxineAppco PharmaOtherNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg recalledVenlafaxine HydrochlorideZydus PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIVenlafaxine Hydrochloride, extended-release capsules recalledThe Harvard Drug GroupPotency & AssayNationwide
DrugCLASS IIVenlafaxine Tablets, USP 50 mg* recalledSUN Pharmaceutical IndustriesOtherTN
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg recalledLucid PharmaPackaging DefectsNationwide
DrugCLASS IIVenlafaxine Hydrochloride extended release capsules, 37.5 mg recalledVenlafaxine HydrochlorideAurobindo Pharma USAOtherNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Capsules, 75 mg recalledGolden State Medical SupplyPotency & AssayNationwide
DrugCLASS IIVenlafaxine HCL ER Capsule USP, 75mg recalledVenlafaxine HydrochlorideZydus Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) recalledGolden State Medical SupplyPotency & AssayNationwide
DrugCLASS IIVenlafaxine HCL ER Capsule USP, 150mg recalledVenlafaxine HydrochlorideZydus Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIIVenlafaxine, Compare to Effexor, a) bottle recalledVenlafaxineBryant Ranch PrepackPackaging DefectsNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg bottles recalledSun Pharma GlobalPotency & AssayNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Tablets, 150 mg recalledCaraco Pharmaceutical LaboratoriesPotency & AssayNationwide
DrugCLASS IVenlafaxine HCl Extended-Release Capsules, 150 mg Unit of Use recalledGreenstonePackaging DefectsNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Tablets, 150 mg recalledCaraco Pharmaceutical LaboratoriesPotency & AssayNationwide
DrugCLASS IIVenlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg recalledCaraco Pharmaceutical LaboratoriesPotency & AssayNationwide
DrugCLASS IIIVenlafaxine Hydrochloride, Extended Release Capsules recalledMcKesson Packaging ServicesPotency & AssayNationwide
DrugCLASS IIVenlafaxine HCL, Tablet, 100 mg recalled by Aidapak ServicesAidapak ServicesLabeling Errors4 states
DrugCLASS IIVenlafaxine HCL ER, Capsule, 150 mg recalled by Aidapak ServicesAidapak ServicesLabeling Errors4 states
DrugCLASS IIVenlafaxine HCL, Tablet, 75 mg recalled by Aidapak ServicesAidapak ServicesLabeling Errors4 states
DrugCLASS IIVenlafaxine HCL, Tablet, 25 mg recalled by Aidapak ServicesAidapak ServicesLabeling Errors4 states
DrugCLASS IIVenlafaxine HCL Tablet, 50 mg recalled by Aidapak ServicesAidapak ServicesLabeling Errors4 states
DrugCLASS IIVenlafaxine Tablet, 25 mg recalled by Aidapak ServicesAidapak ServicesLabeling Errors4 states
DrugCLASS IIVenlafaxine Hydrochloride Tablets, 75 mg* tablets recalledVenlafaxineZydus Pharmaceuticals USAOtherNationwide
DrugCLASS IIIVenlafaxine ER 150mg, 30 Tabs, Generic for: Effexor, Packaged recalledStat Rx USALabeling ErrorsGA, TN

Should you stop taking Venlafaxine?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.