Primal Supplements Group LLC food recall: Primal Herbs
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 98583
- Recall initiated
- Feb 27, 2026
- Classified by FDA
- Oct 21, 2026
- Posted in Enforcement Report
- Oct 28, 2026
- Recalling firm
- PRIMAL SUPPLEMENTS GROUP LLC
- Firm location
- Albuquerque, NM, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Press Release
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Feb 27, 2026. FDA classified it 236 days later, on Oct 21, 2026. Distribution reported by FDA: Product was sold on the website primalherbs.com
Recalled products (1)
H-0172-2027 Class I Ongoing
PRIMAL HERBS, VOLUME, HERBAL SUPPLEMENT, Net Wt. 8.5 oz, 30 servings
Codes / lots: All orders placed between July 2, 2025, and September 19, 2025, on the website: primalherbs.com
Quantity: Unknown
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98583
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.