FDA Drug recall · Reported August 14, 2019
Awake, 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 Awake, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra,… - a moderate-severity action.
Awake, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra,… 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-1589-2019 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-1589-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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 - 2,014 dietary supplements recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.
Product description
Awake, 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-1589-2019 |
| 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-1589-2019) 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.
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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Dietary Supplements · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Compare this recall with Goody King Magnetic Building Cubes and Blocks Recalled Due … → · All Dietary Supplements recalls
Methodology · Corrections · Archive as of August 2026