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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 possible Salmonella contamination. The FDA said no illnesses linked to the recall had been reported; people with the matching bottle should not take the capsules and should discard them.
The U.S. Food and Drug Administration published a recall announcement on October 30 after Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules over possible Salmonella contamination. Routine testing found the potential contamination, and the FDA announcement said no illnesses linked to the recall had been reported at that time.
The recall covers capsules in a 120-count white plastic bottle bearing lot number 2025-26227, UPC 9948252099 and expiration date 10/13/2028. The lot number and expiration date are printed on the bottom of the bottle. Consumers can compare all three identifiers with their product to determine whether it is part of the recall.
The report says the affected lot was sold nationwide at Whole Foods Market stores and on Amazon.com, from November 24, 2025, through October 20, 2026. The product was made by Vitality Works Inc., based in Albuquerque, New Mexico. The FDA announcement described the risk as potential contamination identified during routine sampling; it did not state that every bottle was contaminated.
Consumers who have the matching capsules are advised not to take them and to throw them away rather than return them. The company announcement says customers can seek a refund at any Whole Foods store. Vitality Works listed (505) 268-9950 for questions, with phone hours Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
How to Check Your Bottle
The recall matters because supplements may be kept at home and taken over time, making it possible for consumers to continue using a product after a safety notice. Checking the lot number, UPC and expiration date can help identify whether a bottle is included; the notice applies to the specified lot, not all ashwagandha products or all Whole Foods supplements.
Salmonella infection can cause illness ranging from gastrointestinal symptoms to serious complications. The FDA warning identifies young children, older or frail people, and people with weakened immune systems as groups at greater risk of severe infection. Anyone who has taken the recalled capsules and develops symptoms should contact a health care provider, rather than assuming the illness is unrelated.
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What Testing Prompted the Recall
According to the report, Vitality Works issued the recall after routine sampling of the capsules found they might be contaminated with Salmonella. The FDA published the company’s announcement on October 30. The source material does not describe the sampling method, the number of bottles tested or the precise point in production or distribution where contamination may have occurred.
The notice concerns one named product and one identified lot. Its stated sales period ran from November 2025 to October 2026 through Whole Foods locations and Amazon.com. The recall instruction is to discard the capsules, while the refund option is available at Whole Foods stores, according to the company announcement.
Illness Reports and Contamination Scope
The source report says no illnesses linked to the recall had been reported when it was published. That is a status update, not evidence that no one was exposed or that illness could not be reported later. The available material does not provide a count of affected bottles, explain how many samples tested positive, or say whether investigators identified a specific source of contamination.
It is also not clear from the supplied information whether the FDA or company has issued later updates, whether additional lots are under review, or how many consumers purchased the affected product. The warning is limited to the identified lot unless new information expands its scope.
Steps for Consumers and Retailers
Consumers should check the bottle’s bottom for lot 2025-26227 and expiration date 10/13/2028, then stop using and discard any matching capsules. The company says customers may request a refund at a Whole Foods store; questions can be directed to Vitality Works at (505) 268-9950 during its listed weekday business hours.
Anyone who has taken the capsules and develops fever, diarrhea, nausea, vomiting or abdominal pain should contact a health care provider. The supplied report does not give a date for further updates or identify a next regulatory milestone, so consumers should consult official FDA or company notices for any new information about the recall.
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 with lot number 2025-26227, UPC 9948252099 and expiration date 10/13/2028.
What should I do if I have the recalled bottle?
Do not take the capsules. The company announcement says to throw them away rather than return them. It says customers can get a refund at any Whole Foods store.
What symptoms should I watch for?
The FDA announcement lists fever, diarrhea, nausea, vomiting and abdominal pain; diarrhea may be bloody. Contact a health care provider if symptoms develop after taking the recalled product.
Have any illnesses been reported?
The report said no illnesses linked to the recall had been reported at the time. That status could change, and the supplied material does not include later updates.
Where can I ask questions about the recall?
Vitality Works listed (505) 268-9950 for questions. Its stated phone hours are Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Source: goodhousekeeping.com
