The Recall Desk
ModerateFDA (Drugs)·D-1120-2020·Announced 2020-04-15

Herbal Doctor Remedies Recalls Detoxin-S Capsules Due to CGMP Deviations

Herbal Doctor Remedies is recalling Detoxin-S 500mg capsules because they were found to be misbranded as unapproved new drugs due to CGMP deviations.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically indicates a situation where use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences. The source text does not report any illnesses or injuries, and the hazard is primarily regulatory (misbranding/unapproved new drug) rather than a direct physical safety defect like fire or choking.

Plain-English summary

Herbal Doctor Remedies is voluntarily recalling Detoxin-S, 500mg Capsules, 90-count bottles. The recall was initiated because the products were found to be misbranded as unapproved new drugs, a result of Current Good Manufacturing Practice (CGMP) deviations.

The affected products were sold online within the United States and internationally to Australia, Canada, Israel, Italy, Japan, Norway, and the United Kingdom. The recall covers all lots within their expiry dates.

Consumers who have purchased these products should stop using them and contact Herbal Doctor Remedies at 1(800) 600-0808 for further instructions.

The recalled product

Product
Detoxin-S, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All lots within expiry

Distribution

Distribution scope not specified by the agency.

Part of a larger recall action

This product is one of 70 recalled by Herbal Doctor Remedies under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 70 products in this recall →