Mylan recalls DrNatura Toxinout Kit Broad Spectrum Detoxification Program due to undeclared soy allergen. Consumers should check lot numbers and contact Mylan for details.
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.
“Mylan DrNatura Toxinout Kit Recall: Undeclared Soy Allergen Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17993-mylan-drnatura-toxinout-kit-recall-undeclared-soy-allergen-risk. Based on FDA recall #F-0859-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0859-2019%22&limit=1).
The FDA announced on 2018-12-10 that Mylan Pharmaceuticals Inc. is recalling DrNatura Toxinout Kit Broad Spectrum Detoxification Program due to an undeclared soy allergen, according to the FDA.
How to tell if you have it
Brand: Mylan
Product: DrNatura Toxinout Kit Broad Spectrum Detoxification Program
Item#: 46017-088-18
Lot code: 005983-001
Expiry date: Dec 2018
The hazard
The products are being recalled due to undeclared soy allergen statement, according to the FDA.
Context
GovInfoNow's records show Mylan Pharmaceuticals Inc. has 54 other recalls on record since 2012-06-28. Recent Mylan recalls include Mycophenolate Mofetil Injections (2026-08-26), Prasugrel Tablets (2026-08-17), and Acamprosate Tablets (2026-07-24). Other recent recalls of similar products include ASUKAR TETAS Cherry Milkshake Popsicle Recall (2026-03-11), BEF Foods Park St. Deli Macaroni & Cheese Recall (2026-03-23), and Prospector Popcorn Recall (2026-04-28).
How to tell if you have this one
Check for lot numbers 3020068 (expiry Mar 2019) or 005983-001 (expiry Dec 2018) on the DrNatura Toxinout Kit Broad Spectrum Detoxification Program.
Brand
Mylan
Category
Food
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
US Market
Recall number
Product, codes & lots
Quantity
F-0858-2019
DrNatura Flora Protect¿ Probiotics; Lot 3020068 Item# 46017-088-04
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0859-2019 (December 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0859-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.