Herbal Doctor Remedies Recalls Mental Tonic Capsules for CGMP Violations
Herbal Doctor Remedies is recalling Mental Tonic Capsules because they were manufactured outside of current Good Manufacturing Practice 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 and involves CGMP deviations without reported illnesses or specific high-risk pathogens, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Herbal Doctor Remedies is voluntarily recalling Mental Tonic Capsules. The recall was initiated because the products were manufactured outside of the controls required by current Good Manufacturing Practices (CGMP).
The recalled products were distributed nationwide within the United States and Brazil, as well as on the internet. The recall includes 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
- Mental Tonic Capsules, 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.
See all 43 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 · cgmp deviation
See all →- SevereZicam Cold Remedy Nasal Swabs Recalled for Microbiological Testing Failures
FDA (Drugs) · 2026-09-02
- ModerateGolden State Medical Supply Recalls Carbamazepine Tablets Due to CGMP Deviations
FDA (Drugs) · 2026-08-26
- SevereShoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
FDA (Drugs) · 2026-08-19
- ModerateShoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
FDA (Drugs) · 2026-08-19
- HighShoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
FDA (Drugs) · 2026-08-19