On February 25, 2025, Natural Dior LLC initiated a voluntary nationwide recall of its dietary supplement, Vitafer-L Gold Liquid, after discovering the presence of undeclared tadalafil—a phosphodiesterase (PDE-5) inhibitor used to treat erectile dysfunction. Tadalafil can interact with nitrates found in some prescription medications, potentially causing a significant and life-threatening drop in blood pressure. The recall affects multiple lot numbers with expiration dates ranging from March 2025 to April 2026. The product is packaged in 16.9 fl oz (500 mL) bottles within folding cardboard boxes. To date, no adverse events related to this recall have been reported. Consumers are advised to stop using the product immediately and consult their healthcare provider if they experience any adverse reactions. For more information, consumers can contact Natural Dior LLC's Drug Safety Department at 8:00 am to 5:00 pm EST, Monday through Friday.

News Region:
North America
News Market:
United States of America (USA)
News Tags:
Recall
Dietary supplement
FDA
Health Risk