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Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules after routine testing found potential Salmonella contamination. The FDA announcement says no illnesses linked to the recall had been reported; consumers should not take the capsules and should discard them.
Vitality Works Inc. is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules after routine testing found possible Salmonella contamination, according to a company announcement published by the U.S. Food and Drug Administration on October 30. The capsules were sold nationwide at Whole Foods stores and through Amazon.com; the announcement said no illnesses had been reported in connection with the recall.
The recall covers capsules in a 120-count white plastic bottle. Consumers can identify the product by lot number 2025-26227, UPC 9948252099 and expiration date 10/13/2028. The lot number and expiration date are printed on the bottle’s bottom. The recall does not, according to the source material, include other lots or ashwagandha products.
The report says the affected lot was distributed from November 24, 2025, through October 20, 2026, through Whole Foods stores and Amazon.com. The FDA’s October 30 notice followed routine sampling that found the capsules may be contaminated. The available material does not provide the test results or further detail about how the contamination was detected.
Consumers who have the matching lot should stop taking the capsules and throw them away, rather than return them. The company announcement says consumers may seek a refund at any Whole Foods store. People who have taken the capsules and develop symptoms should contact a health care provider; questions about the recall can be directed to Vitality Works at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Health Risks From Contaminated Capsules
The recall matters because Salmonella can cause gastrointestinal illness and may lead to more serious infections in some people. The FDA announcement identifies young children, older or frail adults, and people with weakened immune systems as groups at greater risk of severe or potentially fatal illness. It also says that, rarely, infection can spread into the bloodstream and cause complications.
Consumers may have purchased the capsules as a supplement rather than as food, so checking the product details is important: the notice concerns a specific lot number and expiration date, not every bottle of ashwagandha. Discarding a matching bottle avoids further exposure while the company and regulators address the recall.
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How to Identify the Recalled Lot
This recall concerns a branded supplement made by Vitality Works Inc. of Albuquerque, New Mexico, and sold under the 365 Whole Foods Market label. The company announcement was published by the FDA on October 30. The stated reason was potential Salmonella contamination found during routine sampling, not a reported cluster of illnesses.
The notice lists three identifiers shoppers can compare with their bottle: lot 2025-26227, UPC 9948252099 and expiration date 10/13/2028. The product was available through two nationwide retail channels, Whole Foods stores and Amazon.com. The source material does not describe other affected products or lots.
Illness Reports and Testing Details
The source report says no illnesses linked to the recall had been reported as of its publication, but it does not give a later case update. It is not clear from the material how many bottles were distributed or whether consumers have reported reactions since the announcement.
The notice identifies routine sampling as the reason for the recall but does not state how many samples tested positive, where sampling took place, or whether the potential contamination was confirmed across the lot. The available information also does not describe any additional lots or products under investigation. Those details should not be inferred from the recall of this single identified lot.
Consumer Actions and Recall Contacts
Consumers should compare the bottom of their bottle with the recall identifiers and discard it if all details match. Do not take the capsules or return them for a refund; the company announcement says a refund is available at any Whole Foods store. Anyone who has taken the product and develops fever, diarrhea, nausea, vomiting or abdominal pain should contact a health care provider promptly.
For questions, consumers can call Vitality Works at (505) 268-9950 during its stated business hours: Monday through Friday, 8 a.m. to 5 p.m. Mountain Time. Further updates, including any change in reported illnesses or the scope of the recall, would need to come from the company or FDA; the source material does not provide a date for another announcement.
Key Questions
Which ashwagandha capsules are included in the recall?
The recall covers 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules in a 120-count white bottle, lot 2025-26227, UPC 9948252099, expiration date 10/13/2028.
What should I do if I have the recalled bottle?
Do not take the capsules. The company announcement instructs consumers to throw them away rather than return them. A refund is available at any Whole Foods store.
What symptoms should I watch for?
The FDA announcement lists fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. Contact a health care provider if symptoms develop after taking the capsules.
Have any illnesses been reported?
The source report says no illnesses linked to the recall had been reported at the time it was published. It does not provide a later update.
Who can answer questions about the recall?
Vitality Works can be reached at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Source: goodhousekeeping.com
