Herbal Doctor Remedies Recalls Lube Lax Capsules for Manufacturing Violations
Herbal Doctor Remedies is recalling Lube Lax Capsules because they were manufactured outside of current Good Manufacturing Practices 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 the source text cites CGMP deviations without reporting specific illnesses or injuries, aligning with the rubric for moderate severity.
Plain-English summary
Herbal Doctor Remedies is voluntarily recalling Lube Lax Capsules. The recall was initiated because the products were manufactured outside of the controls required by current Good Manufacturing Practices (CGMP).
The affected 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 Lube Lax Capsules should stop using the product and contact Herbal Doctor Remedies at 1(800) 600-0808 for further instructions.
The recalled product
- Product
- Lube Lax Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
- Manufacturer
- Herbal Doctor Remedies
- Category
- Drug — Laxative
- 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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