COMPANY ANNOUNCEMENT
VitalityVita Issues Voluntary Nationwide Recall of VitalityXtra and PeakMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac
When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. FDA does not endorse either the product or the company.
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- Company Announcement Date:
- FDA Publish Date:
- Product Type:
- Dietary Supplements
Drugs - Reason for Announcement:
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Recall Reason DescriptionUndeclared Sildenafil and Diclofenac
- Company Name:
- VitalityVita
- Brand Name:
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Brand Name(s)VitalityVita
- Product Description:
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Product DescriptionMarketed as Dietary Supplement
Company Announcement
FOR IMMEDIATE RELEASE – 11/04/24 – Sacramento, CA, VitalityVita.com is voluntarily recalling lot 230811, Exp 8/11/25, of VitalityXtra Capsules and PeakMax Capsules packaged in 10-count blisters in a cardboard carton to the consumer level. VitalityXtra was found to be tainted with sildenafil, an ingredient in FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. PeakMax capsules was found to be tainted with sildenafil and diclofenac, an FDA approved drug known as a nonsteroidal anti-inflammatory drug (NSAID) used to treat pain and inflammation. Products containing sildenafil and diclofenac cannot be marketed as dietary supplements. VitalityVita and PeakMax capsules are unapproved new drugs for which safety and efficacy have not been established and, therefore, subject to recall.
Consumption of products with undeclared sildenafil 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.
Use of products with undeclared diclofenac may cause increased risk of cardiovascular events, such as heart attack and stroke, as well as serious gastrointestinal damage, including bleeding, ulceration, and fatal perforation of the stomach and intestines. This hidden drug ingredient may also interact with other medications and significantly increase the risk of adverse events, particularly when consumers use multiple NSAID-containing products. To date, VitalityVita has not received any reports of adverse events related to this recall.
The products were distributed via the internet at VitalityVita.com nationwide in the USA.
VitalityXtra and PeakMax are marketed as dietary supplements for male performance and energy and are packaged in 10-count blisters packaged in an (VitalityXtra -Green, Yellow White Carton) and (PeakMax in Purple, Yellow and White carton) Lot#: 230811 Exp 8/11/25. The product can be identified by the labels below.
VitalityVita is notifying its distributors and customers by this press announcement and is arranging for return of all recalled products. Please send all returns to 2108 N ST #7929 Sacramento, CA 95816. Consumers that have VitalityXtra or PeakMax capsules lot number 230811 should stop using the product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Consumers with questions regarding this recall can contact VitalityVita via e-mail at vitalityvitacorp@gmail.com Monday through Friday 9AM – 5PM PST.
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.
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
