FDA recall record
DrNatura Toxinout Kit Broad Spectrum Detoxification Program
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 22, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
DrNatura Toxinout Kit Broad Spectrum Detoxification Program
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
DrNatura Toxinout Kit Broad Spectrum Detoxification Program
Code information listed by FDA
Lot 005983-001 Item# 46017-088-18
Distribution and firm information
Recalling firm listed by FDA: Mylan Pharmaceuticals Inc.
Firm location listed by FDA: Morgantown, WV, United States
Distribution reported by FDA: US Market
Product quantity listed by FDA: 800 Kits
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.