Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported August 14, 2019
Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Herbal Doctor Remedies recalled Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Al… - a moderate-severity action.
Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Al… was recalled by Herbal Doctor Remedies in August 14, 2019. Reason: CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Pr…. Check the official notice for the remedy. Verify recall #D-1612-2019 with the FDA Drug before acting.
The recall
Herbal Doctor Remedies issued this moderate-severity FDA Drug recall-CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Pr….
- Moderate
- severity level
- Class II
- classification
- August 14, 2019
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1612-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1612-2019) was formally reported on August 14, 2019, with the manufacturer initiating the action on July 12, 2019. 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: Products were manufactured outside of the controls required by current Good Manufacturing Practices. Distribution data in the federal record shows the product reached: Nationwide within the United States and Brazil and on the internet. 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.
Dietary Supplements recalls over time
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.
Affected scope
N/A
Related Recalls
6
0 from same agency
Product description
Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Reason for recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1612-2019 |
| Date reported | August 14, 2019 |
| Date initiated | July 12, 2019 |
| Recalling firm | Herbal Doctor Remedies |
| Firm location | Monterey Park, CA |
| Affected scope | N/A |
| Distribution | Nationwide within the United States and Brazil and on the internet |
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.
- Check the recall number (D-1612-2019) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
Pain Stopper, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808. Recalled by Herbal Doctor Remedies. Units affected: N/A.
Why was this product recalled? ▼
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 14, 2019. Severity: Moderate. Recall number: D-1612-2019.
Where was the recalled product distributed? ▼
Distribution: Nationwide within the United States and Brazil and on the internet.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1612-2019) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
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 August 14, 2019. 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.