FDA recall record

Herbal Doctor Remedies Worm Off, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies recall — FDA D-1620-2019

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Class IIclassification
D-1620-2019official record ID
Aug 14, 2019report date

Recall record at a glance

Official recordD-1620-2019
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHerbal Doctor Remedies
Report dateAug 14, 2019
Recall initiation dateJul 12, 2019
QuantityN/A
LocationMonterey Park, CA, United States

Official product description

Worm Off, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808

Why the product was recalled

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Distribution information

Nationwide within the United States and Brazil and on the internet

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: N/A.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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