Senna Laxative — Class I drug recall D-0342-2018
Terminated recall by Magno Humphries Laboratories, Inc, reported 2018-02-21, distributed nationwide. Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tab
| Recall number | D-0342-2018 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Magno Humphries Laboratories, Inc, Tigard, OR, United States |
| Recall initiated | 2018-01-17 |
| Classified | 2018-02-09 |
| Reported by FDA | 2018-02-21 |
| Terminated | 2019-12-06 |
| Distributed | Nationwide (US) |
| Quantity | 2,400 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00307610220201 |
| Lot numbers | 01/19, 352300 |
Product
Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.
Reason for recall
Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.
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-0342-2018. 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.