CLASS II Drug recall · Reported 14 Aug 2019 · FDA Enforcement Report
Pain Away recalled by Herbal Doctor Remedies
Herbal Doctor Remedies is recalling Pain Away, distributed nationwide in the US. The recall was initiated on 12 Jul 2019 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1611-2019
- FDA event ID
- 83437
- Recalling firm
- Herbal Doctor Remedies, Monterey Park, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Jul 2019
- FDA classified
- 2 Aug 2019
- Reported
- 14 Aug 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 12 Jul 2019 | Recall initiated by company | |
| 2 Aug 2019 | Classified by FDA | +21 days |
| 14 Aug 2019 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Product as listed by the FDA
Pain Away, 500 mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
Where it was distributed
Nationwide within the United States and Brazil and on the internet
Stores named: Online Retailers
Questions about this recall
Is Pain Away recalled?
Yes. Herbal Doctor Remedies recalled Pain Away on 12 Jul 2019. The recall is Class II and its status is Terminated. Recall number D-1611-2019.
Why was it recalled?
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Which lots are affected?
All lots within expiry
Where was it sold?
Nationwide within the United States and Brazil and on the internet
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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