PRIMAL HERBS, VOLUME, HERBAL SUPPLEMENT, Net Wt. 8.5 oz, 30 servings
Summary
The FDA issued a Class I for PRIMAL HERBS, VOLUME, HERBAL SUPPLEMENT, Net Wt. 8.5 oz, 30 servings by PRIMAL SUPPLEMENTS GROUP LLC. Reason: FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label..
Details
Source
Food Recall
External ID
H-0172-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
PRIMAL HERBS, VOLUME, HERBAL SUPPLEMENT, Net Wt. 8.5 oz, 30 servings
Lot/Code Info: All orders placed between July 2, 2025, and September 19, 2025, on the website: primalherbs.com
Quantity Affected: Unknown
Reason for Recall
FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.
Distribution
Product was sold on the website primalherbs.com
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-27
Company
Albuquerque, NM
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 82 food recalls issued in the same week, part of 117 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (PRIMAL SUPPLEMENTS GROUP LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does PRIMAL SUPPLEMENTS GROUP LLC have FDA actions?
This is the only FDA action we have on record for PRIMAL SUPPLEMENTS GROUP LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0172-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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