Herbal Doctor Remedies Recalls De-Fibroidin Capsules for CGMP Deviations
Herbal Doctor Remedies is recalling De-Fibroidin 500mg capsules because the products 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, and the source text cites misbranding and CGMP deviations without reporting specific illnesses or injuries, fitting the criteria for moderate severity.
Plain-English summary
Herbal Doctor Remedies is recalling De-Fibroidin, 500mg Capsules, 90-count bottles. The recall was initiated because the products have been found to be misbranded as unapproved new drugs due to 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. All lots within the expiry date are included in this recall.
Consumers should stop using the product and contact Herbal Doctor Remedies at 1(800) 600-0808 for further instructions.
The recalled product
- Product
- De-Fibroidin, 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 — Dietary 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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