Herbal Doctor Remedies Recalls Edema Off Capsules for Manufacturing Violations
Herbal Doctor Remedies is recalling Edema Off Capsules because they were manufactured outside of current Good Manufacturing Practices (CGMP) controls.
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 involves a reasonable probability of temporary or medically reversible adverse health consequences. The specific hazard is a CGMP deviation, which is a process violation rather than a confirmed contamination or injury event, fitting the Moderate severity criteria for voluntary precautionary recalls or minor labeling/process errors.
Plain-English summary
Herbal Doctor Remedies is voluntarily recalling Edema Off Capsules. The product was distributed nationwide within the United States, in Brazil, and on the internet. The recall involves all lots within their expiry dates.
The recall was initiated because the products were manufactured outside of the controls required by current Good Manufacturing Practices (CGMP). This indicates that the manufacturing process did not adhere to the necessary quality and safety standards.
Consumers who have purchased Edema Off Capsules should stop using the product and contact Herbal Doctor Remedies at 1(800) 600-0808 for further instructions or a refund.
The recalled product
- Product
- Edema Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
- Manufacturer
- Herbal Doctor Remedies
- Category
- Drug — Dietary Supplement
- Hazard
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
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 43 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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