The Recall Desk
ModerateFDA (Drugs)·D-1619-2019·Announced 2019-08-14

Herbal Doctor Remedies Recalls Vertigo Off Capsules for Manufacturing Deviations

Herbal Doctor Remedies is recalling Vertigo Off Capsules because they were manufactured outside of required 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, which typically indicates a situation where use of the product could cause temporary or medically reversible health consequences. The source text cites CGMP deviations without reporting specific illnesses or injuries, aligning with a Moderate severity rating for a voluntary precautionary recall.

Plain-English summary

Herbal Doctor Remedies is voluntarily recalling Vertigo Off Capsules. The product was distributed nationwide within the United States, in Brazil, and on the internet. The recall covers all lots within their expiration dates.

The recall was initiated because the products were manufactured outside of the controls required by current Good Manufacturing Practices (CGMP). This deviation from standard manufacturing protocols is the specific reason for the recall action.

Consumers who have purchased Vertigo Off Capsules should stop using the product. They can contact Herbal Doctor Remedies at 1(800) 600-0808 for further information or to arrange a return.

The recalled product

Product
Vertigo Off Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Manufacturer
Herbal Doctor Remedies
Category
Drug — 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 →

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