Brand Family

Herbalife Products in FDA Data

Individual FDA adverse event report counts for Herbalife product variants. Counts are per-product — they are never combined across SKUs.

These are reports submitted to the FDA. A report does not mean any product caused the effect. Each SKU's count is tracked individually and is never summed across variants.

Herbalife Product Variants

Each entry is a distinct product as named in FDA reports. Click any product to see its full adverse event breakdown.

Herbalife Cell Activator 86 reports · 2007–2022
Herbalife Cell-u-loss 63 reports · 2008–2021
Herbalife Total Control 63 reports · 2004–2024
Herbalife Herbal Aloe Concentrate 38 reports · 2009–2022
Herbalife Multivitamin Complex Formula 2 35 reports · 2008–2012
Herbalife Florafiber 32 reports · 2006–2018
Herbalife Herbal Tea Concentrate 31 reports · 2007–2022
Herbalife Thermo-bond 29 reports · 2007–2020
Herbalife Formula 1 28 reports · 2009–2015
Herbalife Aminogen 26 reports · 2007–2019
Herbalife Snack Defense 26 reports · 2008–2022

Data Source

Data from FDA's CFSAN Adverse Event Reporting System (CAERS). Reports are voluntary submissions — they do not establish that any product caused any event.

View openFDA CAERS source ↗ · About our methodology