The Recall Desk
HighFDA (Drugs)·D-1609-2019·Announced 2019-08-14

Herbal Doctor Remedies Recalls Lung Tonic EX Capsules for Manufacturing Deviations

Herbal Doctor Remedies is recalling Lung Tonic EX Capsules because they were manufactured outside of required Good Manufacturing Practices controls.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II, which typically involves a risk of temporary or medically reversible adverse health consequences. The source text does not report specific injuries or illnesses, placing this in the 'High' category for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Herbal Doctor Remedies is recalling Lung Tonic EX Capsules. The product was distributed nationwide within the United States and Brazil, as well as on the internet. The recall covers all lots within their expiry dates.

The FDA identified that the products were manufactured outside of the controls required by current Good Manufacturing Practices (CGMP). This classification indicates a potential risk of harm, though the source text does not specify reported illnesses or injuries.

Consumers who have purchased Lung Tonic EX Capsules should stop using the product. They can contact Herbal Doctor Remedies at 1(800) 600-0808 for further information regarding the recall.

The recalled product

Product
Lung Tonic EX Capsules, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

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 →