Herbal Doctor Remedies Recalls Nasal Ez Capsules Due to Misbranding
Herbal Doctor Remedies is recalling Nasal Ez capsules because they 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 involves a temporary or medically reversible adverse health consequence. The specific hazard is misbranding as an unapproved new drug, which aligns with moderate severity criteria for regulatory compliance issues without reported acute physical injury.
Plain-English summary
Herbal Doctor Remedies is recalling Nasal Ez, 500mg capsules in 90-count bottles. The recall was initiated because the products were found to be misbranded as unapproved new drugs.
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 expiration 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
- Nasal Ez, 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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