ACTIVE RECALL — CLASS IActive recallH-0172-2027/FDA enforcement

Primal Herbs, Volume, Herbal Supplement, NET WT

What you need to know

Class I
  • What happened

    FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A prescription drug ingredient hidden in a product sold as a supplement or food, creating serious cardiac risks.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Active recall · classified by the FDADistribution not listedMore supplements

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Match before you discard

Product identification

Source: FDA FOOD

Brand namePrimal Supplements Group LLC
Recalling firmPrimal Supplements Group LLCAlbuquerque, NM, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • All orders placed between July 2, 2025, and September 19, 2025, on the website: primalherbs.com
Distribution area

Product was sold on the website primalherbs.com

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: October 28, 2026
FDA recall numberH-0172-2027

Beyond the headline

The recall, in context

Primal Supplements Group LLC initiated this supplements recall on February 27, 2026. The FDA enforcement report states: FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label. The FDA report lists distribution as: Product was sold on the website primalherbs.com.

The FDA enforcement report describes the reason as: FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.

Primal Herbs, Volume, Herbal Supplement, NET WT was made or distributed by Primal Supplements Group LLC in Albuquerque, NM, United States. This page reflects FDA report H-0172-2027, dated October 28, 2026.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a prescription drug ingredient hidden in a product sold as a supplement or food, creating serious cardiac risks.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Primal Herbs, Volume, Herbal Supplement, NET WT recall?

Primal Supplements Group LLC recalled Primal Herbs, Volume, Herbal Supplement, NET WT in an FDA Class I enforcement action reported as H-0172-2027. FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil not listed on the product label.

What are the symptoms of Product safety recall exposure?

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

How do I get a refund from Primal Supplements Group LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0172-2027 and keep the packaging, lot code and proof of purchase if you have them.

Is the Primal Supplements Group LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0172-2027. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Related alerts

Recent Undeclared sildenafil recalls

All alerts

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.