FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Mylan Pharmaceuticals DrNatura Toxinout Kit Broad Spectrum Recall

DrNatura Toxinout Kit Broad Spectrum Detoxification Program

Mylan Pharmaceuticals Inc. · Morgantown, WV

Risk level
Class II
Reported by FDA
Feb 20, 2019
Recall ID
F-0859-2019
Check your lot numberHow we source this data

Summary

Mylan Pharmaceuticals recalled DrNatura Toxinout Kit Broad Spectrum starting Dec 10, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0859-2019 on Feb 20, 2019. Reason: 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. Status: Terminated.

Why it was recalled

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.

Product description

DrNatura Toxinout Kit Broad Spectrum Detoxification Program

Lot numbers, UPCs & expiration codes

Lot 005983-001 Item# 46017-088-18

Where it was sold

US Market

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0859-2019
Classification
Class II
Status
Terminated
Recall initiated
Dec 10, 2018
FDA report date
Feb 20, 2019
Quantity
800 Kits
Recall type
Voluntary: Firm initiated
Recalling firm
Mylan Pharmaceuticals Inc.

Original FDA data

Every field from FDA enforcement report F-0859-2019, exactly as published.

Show all FDA fields
City
Morgantown
State
WV
Status
Terminated
Country
United States
Event ID
81774
Address
781 Chestnut Ridge Rd
Code information
Lot 005983-001 Item# 46017-088-18
Postal code
26505-2730
Report date
Feb 20, 2019
Product type
Food
Recall number
F-0859-2019
Classification
Class II
Recalling firm
Mylan Pharmaceuticals Inc.
Product quantity
800 Kits
Termination date
Oct 22, 2019
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
DrNatura Toxinout Kit Broad Spectrum Detoxification Program
Distribution pattern
US Market
Recall initiation date
Dec 10, 2018
Initial firm notification
Letter
Center classification date
Feb 8, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0859-2019, published Feb 20, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls