F-0859-2019 Class II Terminated

Recalled by Mylan Pharmaceuticals Inc. — Morgantown, WV

FDA food recall F-0859-2019 was initiated by Mylan Pharmaceuticals Inc. on Dec 10, 2018 and is designated Class II. 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… The recall status is terminated (terminated Oct 22, 2019). Affected quantity: 800 Kits.

Recall Details

Product Type
Food
Report Date
Feb 20, 2019
Initiation Date
Dec 10, 2018
Termination Date
Oct 22, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
800 Kits

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.

Distribution Pattern

US Market

Code Information

Lot 005983-001 Item# 46017-088-18

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0859-2019
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 6, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.