Herbal Doctor Remedies Recalls Asma Stopper Capsules for Misbranding
Herbal Doctor Remedies is recalling Asma Stopper capsules because they are 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 corresponds to a moderate severity level. The hazard involves misbranding as an unapproved new drug, which is a regulatory violation without explicit reports of immediate physical injury in the source text.
Plain-English summary
Herbal Doctor Remedies is recalling Asma Stopper, 500mg capsules in 90-count bottles. The recall is due to Current Good Manufacturing Practice (CGMP) deviations, specifically that the products have been 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. All lots within the expiry date are included in this recall.
Consumers who purchased Asma Stopper capsules should stop using the product and contact Herbal Doctor Remedies at 1(800) 600-0808 for further instructions.
The recalled product
- Product
- Asma Stopper, 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 — Unapproved New Drug
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 →Related recalls
Same manufacturer · Herbal Doctor Remedies
See all →- ModerateHerbal Doctor Remedies Recalls Max Slim Capsules for Misbranding
FDA (Drugs) · 2020-04-15
- SevereHerbal Doctor Remedies Recalls Herpes Off Due to Unapproved New Drug Status
FDA (Drugs) · 2020-04-15
- ModerateHerbal Doctor Remedies Recalls Voice Rescue Capsules Due to Misbranding
FDA (Drugs) · 2020-04-15
- SevereHerbal Doctor Remedies Recalls Lipidtrol Capsules for CGMP Deviations
FDA (Drugs) · 2020-04-15
- SevereHerbal Doctor Remedies Recalls Thyro-H Capsules for CGMP Deviations
FDA (Drugs) · 2020-04-15
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02