CLASS I ONGOING Food recall · Reported 28 Oct 2026 · FDA Enforcement Report
Primal Herbs, Volume, Herbal Supplement recalled
Primal Supplements Group is recalling Primal Herbs, Volume, Herbal Supplement. The recall was initiated on 27 Feb 2026 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0172-2027
- FDA event ID
- 98583
- Recalling firm
- Primal Supplements Group, Albuquerque, NM
- Brand
- Primal Herbs
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 27 Feb 2026
- FDA classified
- 21 Oct 2026
- Reported
- 28 Oct 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
- Product category
- Herbal Supplements
Timeline
| 27 Feb 2026 | Recall initiated by company | |
| 21 Oct 2026 | Classified by FDA | +236 days |
| 28 Oct 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
PRIMAL HERBS, VOLUME, HERBAL SUPPLEMENT, Net Wt. 8.5 oz, 30 servings
Where it was distributed
Product was sold on the website primalherbs.com
Questions about this recall
Why was it recalled?
FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
Which lots are affected?
All orders placed between July 2, 2025, and September 19, 2025, on the website: primalherbs.com
Where was it sold?
Product was sold on the website primalherbs.com
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 3 Nov 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Herbal Supplements recalls
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|---|---|---|---|---|---|
| Food | ANNOUNCED | 365 Whole Foods Market Standardized + Full Spectrum Blend recalled365 Whole Foods Market | Vitality Works | Salmonella | 31 states |
| Food | CLASS III | American Ginsengs recalled by Kwok Shing | Kwok Shing | Other | CA |
| Food | CLASS I | organic moringa leaf powder recalled by Foods Alive | Foods Alive | Salmonella | Nationwide |
| Food | CLASS I | Lacnola; Small recalled by The Hampton Grocer | The Hampton Grocer | Salmonella | Nationwide |
| Food | CLASS II | A-L Complex Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |