FDA recall, , High risk
Primal Herbs Volume Herbal Supplement
Primal Herbs Volume herbal supplement contains undeclared sildenafil, which may lower blood pressure to dangerous levels.
Summary by Recall Canary from the FDA notice
What happened
Primal Supplements Group LLC of Albuquerque, New Mexico, voluntarily recalled all orders of Primal Herbs Volume placed between July 2 and September 19, 2025, because FDA laboratory analysis confirmed the supplement contains sildenafil not listed on the product label. The product, sold on the website primalherbs.com, is an herbal supplement with net weight 8.5 ounces and 30 servings.
The company began the recall on February 27, 2026, and the FDA added it to its Enforcement Report on October 21, 2026.
What to do
If you have this product:
- Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this product.
- Customers who placed an order between July 2, 2025 and September 19, 2025, on the website: primalherbs.com, should discontinue use immediately.
- If your order was placed during this timeframe, please stop using the product and contact our team at hello@
primalherbs.com with your order number. - For questions or concerns, please contact hello@
primalherbs.com or +1 (856) 420-6117.
Is yours affected?
Compare these details with yours, then check the recall notice to see which units are recalled.
Primal Herbs, Volume, Herbal Supplement, Net wt. 8.5 oz, 30 Servings
- Affected units
- All orders placed between July 2, 2025, and September 19, 2025, on the website: primalherbs.com
Recall details
- Company began the recall
- Sold in
Product was sold on the website primalherbs.com
- Company
- PRIMAL SUPPLEMENTS GROUP LLC
- Hazard
- Hidden drug ingredient
- Risk
High risk
There is a reasonable chance that eating it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98583
- Recall number
- H-0172-2027
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall · Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
Summary updated
