Severity
Moderate
FDA Drug recall · Reported April 15, 2020
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
Herbal Doctor Remedies recalled Acupuncture, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 60… - a moderate-severity action.
Acupuncture, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 60… was recalled by Herbal Doctor Remedies in April 15, 2020. Reason: CGMP Deviations: These products have been found to be misbranded as unapproved new drugs. Check the official notice for the remedy. Verify recall #D-1105-2020 with the FDA Drug before acting.
The recall
Herbal Doctor Remedies issued this moderate-severity FDA Drug recall-CGMP Deviations: These products have been found to be misbranded as unapproved new drugs.
Sourced from official FDA Drug enforcement records. Verify recall #D-1105-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1105-2020) was formally reported on April 15, 2020, with the manufacturer initiating the action on March 24, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Herbal Doctor Remedies is listed as the recalling firm, operating out of Monterey Park, CA. Federal records list the affected scope as N/A.
The documented reason for this recall is: CGMP Deviations: These products have been found to be misbranded as unapproved new drugs Distribution data in the federal record shows the product reached: Products are sold online within the United States and internationally to the following countries: Australia, Canada, Israel, Italy, Japan, Norway, and United Kingdom. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
N/A
Related Recalls
6
0 from same agency
Acupuncture, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
CGMP Deviations: These products have been found to be misbranded as unapproved new drugs
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1105-2020 |
| Date reported | April 15, 2020 |
| Date initiated | March 24, 2020 |
| Recalling firm | Herbal Doctor Remedies |
| Firm location | Monterey Park, CA |
| Affected scope | N/A |
| Distribution | Products are sold online within the United States and internationally to the following countries: Australia, Canada, Israel, Italy, Japan, Norway, and United Kingdom |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Winder Laboratories, LLC · 2026-03-25
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported April 15, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.