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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted February 27, 2025
Male Enhancement Supplement Sold on Amazon and Walmart Recalled
On February 25, 2025, Natural Dior LLC recalled affected lots of a dietary supplement Vitafer-L Gold Liquid because it contains undeclared tadalafil, which is not permitted in dietary supplements.
(See ConsumerLab's Sexual Enhancer Supplements Review for tests of related products.)
Tadalafil (the active ingredient in Cialis) is prescribed for erectile dysfunction. It can cause symptoms like headache and flushing and can interact with medications containing nitrates such as nitroglycerine, resulting in dangerously low blood pressure.
Recalled Vitafer-L Gold Liquid (see product photos) was sold nationwide through Amazon and Walmart. It is packaged in 16.9 fl oz (1.06 pt) 500 mL bottles in a folding cardboard box and can further be identified by the following 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
Consumers who purchased the recalled products should immediately discontinue use of the product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these drug products.
Consumers and healthcare providers can report any adverse reactions to the FDA's MedWatch Voluntary Reporting Program.
For more information, use the link below.
See related recalls and warnings:
Vitality Sexual Enhancement Supplement Recalled
Two Sexual Enhancement Supplements Sold on Amazon Recalled
Sustain and Schwinnng Male Enhancement Supplements Recalled
Three Male Enhancement Products Recalled Due to Undeclared Drugs
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
Please complete the form below as accurately as possible. You may need to check the label on the product.
Thank you for submitting your report.
Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
Thank you for submitting your report.
