DrNatura Toxinout Kit Broad Spectrum Detoxification Program — Class II food recall F-0859-2019
Terminated recall by Mylan Pharmaceuticals Inc., reported 2019-02-20. Mylan Consumer Healthcare has decided to initiate recall of the following products : Item# 46017-088-04 DrNatu
| Recall number | F-0859-2019 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mylan Pharmaceuticals Inc., Morgantown, WV, United States |
| Recall initiated | 2018-12-10 |
| Classified | 2019-02-08 |
| Reported by FDA | 2019-02-20 |
| Terminated | 2019-10-22 |
| Quantity | 800 kits |
| Reason classes | undeclared allergen |
| Allergens | soy |
| NDC | 46017-0088-18 |
| Lot numbers | 005983-001, 46017-088-18 |
| Model numbers | 46017-088-18 |
Product
DrNatura Toxinout Kit Broad Spectrum Detoxification Program
Reason for recall
Mylan Consumer Healthcare has decided to initiate recall of the following products : Item# 46017-088-04 DrNatura Flora Protect Probiotics lot 3020068 Expiry Mar 2019 and Item# 46017-088-18 DrNatura Toxinout Kit lot 005983-001 Expiry Dec 2018 . The products are being recalled due to undeclared soy allergen statement.
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/F-0859-2019. 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.