DrNatura Toxinout Kit Broad Spectrum Detoxification Program

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# 46…

Recall #: F-0859-2019
Affected scope: 800 Kits
Initiated: December 10, 2018

Compiled from official public sources by the publisher. · Updated September 2026

Verify with FDA Food →

View my saved recalls

Mylan Pharmaceuticals Inc. recalled DrNatura Toxinout Kit Broad Spectrum Detoxification Program - a moderate-severity action.

DrNatura Toxinout Kit Broad Spectrum Detoxification Program was recalled by Mylan Pharmaceuticals Inc. in February 20, 2019. Reason: Mylan Consumer Healthcare has decided to initiate recall of the following products : Item# 46017-088-04 DrNa…. Check the official notice for the remedy. Verify recall #F-0859-2019 with the FDA Food before acting.

The recall

Mylan Pharmaceuticals Inc. issued this moderate-severity FDA Food recall-Mylan Consumer Healthcare has decided to initiate recall of the following products : Item# 46017-088-04 DrNa….

Moderate
severity level: Class II
classification: February 20, 2019
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0859-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

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.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-0859-2019
Date reported	February 20, 2019
Date initiated	December 10, 2018
Recalling firm	Mylan Pharmaceuticals Inc.
Firm location	Morgantown, WV
Affected scope	800 Kits
Distribution	US Market

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-0859-2019) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

DrNatura Toxinout Kit Broad Spectrum Detoxification Program. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 800 Kits.

Why was this product recalled? ▼

Which agency issued this recall? ▼

This recall was issued by the FDA Food on February 20, 2019. Severity: Moderate. Recall number: F-0859-2019.

Where was the recalled product distributed? ▼

Distribution: US Market.

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

Crate and Barrel Recalls Holiday Milk Bot… 2019-02-20 Acetylcysteine Ophthalmic Solution, 100mg… 2019-02-20 Prednisolone and Moxifloxacin Ophthalmic … 2019-02-20 Prednisolone and Gatifloxacin Ophthalmic … 2019-02-20

Similar Food · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

The Forest Wild Collection Dark Chocolate… 2019-02-20 Culinary Secrets, Butterscotch Instant Pu… 2019-02-20 Chocolate instant pudding and pie filling… 2019-02-20 Vanilla instant pudding and pie filling p… 2019-02-20

Compare this recall with Grade A White In-shell Chicken eggs packaged in the followi… → · All Food recalls

This recall: FDA Food, reported February 20, 2019. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026