Herbal Doctor Remedies Recalls Lipidtrol Capsules for CGMP Deviations
Herbal Doctor Remedies is recalling Lipidtrol 500mg capsules because the products were found to be misbranded as unapproved new drugs due to CGMP deviations.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class II, which corresponds to a Severe rating (score 4) under the provided rubric.
Plain-English summary
Herbal Doctor Remedies is recalling Lipidtrol, 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 distributed by Herbal Doctor Remedies in Alhambra, California. The products were sold online within the United States and internationally to Australia, Canada, Israel, Italy, Japan, Norway, and the United Kingdom. All lots within expiry are included in this recall.
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
- Lipidtrol, 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 — 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.
See all 70 products in this recall →Related recalls
Same manufacturer · Herbal Doctor Remedies
See all →- SevereHerbal Doctor Remedies Recalls Thyro-H Capsules for CGMP Deviations
FDA (Drugs) · 2020-04-15
- ModerateHerbal Doctor Remedies Recalls DeTensin Ex for Unapproved New Drug Status
FDA (Drugs) · 2020-04-15
- ModerateHerbal Doctor Remedies Recalls Voice Rescue Capsules Due to Misbranding
FDA (Drugs) · 2020-04-15
- ModerateHerbal Doctor Remedies Recalls Max Slim Capsules for Misbranding
FDA (Drugs) · 2020-04-15
- ModerateHerbal Doctor Remedies Recalls Vertigo Off Due to Unapproved New Drug Status
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