Detox Transforms Recalls — U.S. Recall Records

Recall history in this database

Classification mix: Class I: 5.

DrugMay 13, 2015

Detox Transforms AMPD GOLD Bee Pollen capsules, 350 mg, 60-count bottle, Signature, 1027 recall — FDA D-0979-2015

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil, making AMPD GOLD an unapproved drug.

Class IFDA: TerminatedDetox Transforms

DrugMay 13, 2015

Detox Transforms iNSANE Bee Pollen capsules, 200 mg, 60-count bottle, Developed by recall — FDA D-0981-2015

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making iNSANE an unapproved drug.

Class IFDA: TerminatedDetox Transforms

DrugMay 13, 2015

Detox Transforms EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed recall — FDA D-0977-2015

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making EDGE an unapproved drug.

Class IFDA: TerminatedDetox Transforms

DrugMay 13, 2015

Detox Transforms BtRiM Max capsules, 60-count bottle, Developed by Signature, 1027 Highway recall — FDA D-0980-2015

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein, making BtRiM Max an unapproved drug.

Class IFDA: TerminatedDetox Transforms

DrugMay 13, 2015

Detox Transforms iNDiGO capsules, 220 mg, 60-count bottle, Developed by Signature, 1027 recall — FDA D-0978-2015

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein, making iNDiGO an unapproved drug.

Class IFDA: TerminatedDetox Transforms

Understanding this recall history

This page summarizes recall records in which the official source identifies Detox Transforms as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.