Herbal Doctor Remedies Recalls Reman-6 Capsules Due to CGMP Deviations
Herbal Doctor Remedies is recalling Reman-6 500mg capsules because the products were found to be misbranded as unapproved new drugs.
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 the product may cause temporary or medically reversible adverse health consequences. The source text does not report any illnesses or injuries, and the hazard is related to regulatory misbranding rather than a specific physical or biological contamination.
Plain-English summary
Herbal Doctor Remedies is recalling Reman-6, 500mg capsules, 90-count bottles. The recall was initiated because the products have been found to be misbranded as unapproved new drugs, which constitutes a Current Good Manufacturing Practice (CGMP) deviation.
The affected products were distributed by Herbal Doctor Remedies in Alhambra, California. The products were sold online within the United States and internationally to Australia, Canada, Israel, Italy, Japan, Norway, and the United Kingdom. The recall includes all lots within their expiry dates.
Consumers who have purchased Reman-6 capsules should stop using the product and contact Herbal Doctor Remedies at 1(800) 600-0808 for further instructions.
The recalled product
- Product
- Reman-6, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
- Manufacturer
- Herbal Doctor Remedies
- Category
- Drug — Supplement
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.
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