Elevated risk U.S. Food and Drug Administration

Natural Dior Dietary Supplement recall: Undeclared Tadalafil

Recall published 1+ years ago

Undeclared Tadalafil

Natural Dior Dietary supplements — recalled dietary supplements
Photo published by U.S. Food and Drug Administration with the recall notice.

The hazard: Undeclared allergen or ingredient

The food itself is fine. What is wrong is the label, and for the households that rely on that label it is a real risk.

What the notice says: Risk Statement: Consumption of products with undeclared tadalafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening.

Why it matters: An ingredient that U.S. law requires to be declared is present but missing from the label. People who avoid that ingredient cannot make a safe choice from the packaging.

Symptoms and when to call a doctor

An undeclared allergen is a danger only to people allergic or intolerant to that ingredient. For everyone else the food is safe. Reactions range from an itchy mouth, hives, stomach cramps or vomiting through to anaphylaxis — swelling of the lips, tongue or throat, a tight chest, wheezing, a sudden drop in blood pressure or collapse. If anaphylaxis is suspected, use an epinephrine auto-injector straight away and call 911, even if the symptoms seem to settle, because a second wave can follow hours later.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Published
February 25, 2025
Risk level
Elevated risk
Issued by
U.S. Food and Drug Administration
Brand
Natural Dior
Product type
Dietary supplements
Distribution
Nationwide
Sold at
Walmart, Amazon
Reports of harm
No adverse reactions have been reported to Natural Dior LLC (USA) as of February 20, 2025

Products covered by this recall

Dietary Supplement

What the company announced

FOR IMMEDIATE RELEASE - Natural Dior LLC (USA) – February 25, 2025 – Natural Dior LLC, is voluntarily recalling the affected lots of Vitafer-L Gold Liquid , a dietary supplement with iron and vitamins, to the consumer level. The product has been found to contain undeclared tadalafil , an ingredient in FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. Products containing tadalafil cannot be marketed as dietary supplements. Vitafer-L Gold Liquid is an unapproved new drugs for which safety and efficacy have not been established and, therefore, subject to recall.

Risk Statement: Consumption of products with undeclared tadalafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk. To date, Natural Dior LLC has not received any reports of adverse events related to this recall .

The product is used as a state indication(s) and is packaged in 16.9 fl oz (1.06 pt) 500 mL bottles in a folding cardboard box.

Lot Numbers and Expiration Dates: Lot 7021-2304 – Exp. April 2025

Lot 7017-2304 – Exp. April 2025

Lot 7040-2305 – Exp. May 2025

Lot 10020-2402 – Exp. February 2026

Lot 10011-2404 – Exp. April 2026

Lot 7695-2307 – Exp. Not specified

Lot R6715-2303 – Exp. March 2025

Lot 7292-2305 – Exp. May 2025

Lot 9669-2403 – Exp. March 2025

Lot 10060-2404 – Exp. April 2026

The product was sold nationwide via Amazon and Walmart and distributed through wholesale accounts . The product was also exported to Miami, Florida, through an importer (Laboratorio Natural Dior LLC) .

Consumers who have purchased this product should stop using it immediately and dispose of it properly or return it to the place of purchase for a refund.

Consumers with questions regarding this recall can contact Natural Dior LLC at +57 315 2814091 from 10AM - 5PM or via email at [email protected] .

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting Program either online, by regular mail, or by fax. No adverse reactions have been reported to Natural Dior LLC (USA) as of February 20, 2025

Online : www.fda.gov/medwatch

Mail : Download the form at www.fda.gov/MedWatch/getforms.htm and send it to the address on the form.

Fax : 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration .

Natural Dior LLC is committed to ensuring the safety and quality of its products and is taking all necessary steps to remove the affected product from the market.

Reproduced from the company announcement posted on fda.gov. Links and contact forms in the original are not repeated here; the official notice below has them.

Check your product

The notice names 17 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 7021-2304
  • 7017-2304
  • 7040-2305
  • 10020-2402
  • 10011-2404
  • 7695-2307
  • R6715-2303
  • 7292-2305
  • 9669-2403
  • 10060-2404

Best-by / use-by date

Printed beside the lot code, not on the price sticker.

  • April 2025
  • May 2025
  • February 2026
  • April 2026
  • March 2025

Package size

Match the net weight or the piece count on the front of the pack.

  • 16.9 fl oz
  • 500 mL

Codes are lifted verbatim from the FDA — Company recall announcements notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Allergen

Natural Dior — The food itself is fine. What is wrong is the label, and for the households that rely on that label it is a real risk.

  1. Read the official notice above for the exact ingredient involved, then check whether anyone in your home avoids it.
  2. Warn anyone else who eats from your kitchen, including schools and childminders.
  3. Report any reaction to the FDA so it is recorded against this recall.
  4. If nobody here avoids it, the product is safe to eat; the refund is still available if you would rather return it.

Getting a refund without the pack

The commonest reason people skip the refund is that they have already thrown the item away. That rarely matters.

  • A photo of the label and lot code is accepted by most grocers, and so is a card statement line showing the purchase.
  • Store credit is often offered first. You can ask for the original payment method instead, and it is normally granted.
  • No photo either? Ask anyway. Grocery chains settle recall refunds at the service desk because disputing them costs more than paying them.
  • For a multi-pack or a case, ask for the full purchase price rather than a per-unit figure — the recall covers what you paid.

Remedy named in the notice: Consumers who have purchased this product should stop using it immediately and dispose of it properly or return it to the place of purchase for a refund.

Company contact: Natural Dior LLC — Consumers: +57 315 2814091, [email protected] — Media: Victor Diaz, Natural Dior LLC, [email protected]

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Company recall announcements record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Natural Dior dietary supplements recalled?

Undeclared Tadalafil Risk Statement: Consumption of products with undeclared tadalafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: lot code 7021-2304, 7017-2304, 7040-2305; best-by date April 2025 or May 2025. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Read the official notice above for the exact ingredient involved, then check whether anyone in your home avoids it.

Can I get my money back?

The notice says: Consumers who have purchased this product should stop using it immediately and dispose of it properly or return it to the place of purchase for a refund.

Where was the recalled product sold?

It was distributed nationwide, including at Walmart, Amazon.

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