VERMOX Tablets 100 mg — Class II drug recall D-1041-2016
Terminated recall by Profarma Distributors LLC, reported 2016-06-29, distributed nationwide. CGMP Deviations
| Recall number | D-1041-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Profarma Distributors LLC, Columbus, OH, United States |
| Recall initiated | 2016-05-11 |
| Classified | 2016-06-17 |
| Reported by FDA | 2016-06-29 |
| Terminated | 2017-01-24 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 07501109900619 |
| Lot numbers | 08/17, UPE187 |
Product
VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619
Reason for recall
CGMP Deviations
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-1041-2016. 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.