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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. No illnesses linked to the recall have been reported, according to the source report; consumers should not take the capsules and should discard them.
The U.S. Food and Drug Administration published a recall announcement on October 30 for one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules, after routine testing found possible Salmonella contamination. The recall was issued by Vitality Works Inc.; the capsules were sold at Whole Foods stores and on Amazon.com, and no illnesses linked to the recall had been reported in the source report.
The affected product is sold in a 120-count white plastic bottle. Consumers can identify it 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 applies to this lot, not every ashwagandha product or all Whole Foods supplements.
The capsules were distributed nationwide through Whole Foods stores and Amazon.com. The source report gives the sales period as November 24, 2025, through October 20, 2026. It also describes distribution as running from November 2025 through October 2026. Those dates are presented as stated in the report; the year of the October 30 FDA announcement is not specified in the supplied material.
Consumers who have the identified bottles are advised not to take the capsules and to throw them away rather than return them. The company announcement says customers can seek a refund at any Whole Foods store. For questions, Vitality Works lists (505) 268-9950, with phone hours Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Salmonella Risk and Consumer Actions
The recall matters because Salmonella infection can cause gastrointestinal illness and, in some cases, more serious complications. The FDA announcement says symptoms can include fever, diarrhea, nausea, vomiting and abdominal pain. It warns that young children, frail or older adults, and people with weakened immune systems may be at greater risk of severe infection.
The alert gives shoppers a way to distinguish the affected stock from other supplements by its lot number, UPC and expiration date. Checking the bottom of the bottle can help consumers avoid taking a product identified in the recall. People who have used the capsules and develop symptoms should contact a health care provider, according to the recall guidance.
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How the Capsule Lot Was Identified
According to the report, the possible contamination was identified through routine sampling. Vitality Works Inc., based in Albuquerque, New Mexico, recalled the lot, and the FDA published the company’s announcement. The supplied material does not describe the specific testing method or provide laboratory results beyond stating that routine testing found the capsules may be contaminated.
The notice concerns a particular supplement product and a single identified lot. It does not say that all ashwagandha supplements, all products made by Vitality Works, or other 365-branded items are affected. Consumers should use the listed product identifiers rather than relying on the brand name alone.
Illness Reports and Recall Scope
The source report says no illnesses linked to the recall had been reported at the time it was written. That does not establish whether anyone may have become ill but had not yet reported it, and the supplied material gives no later case count or investigation update.
The source information also leaves some timing details unresolved: it gives an October 30 announcement date without a year while listing sales dates extending through October 20, 2026. It does not state how many bottles were distributed, whether all affected units have been accounted for, or whether additional lots are being evaluated.
Check Bottles and Follow Recall Updates
Consumers should compare any bottle of the product against the 2025-26227 lot number, UPC 9948252099 and 10/13/2028 expiration date. If all identifiers match, do not use the capsules; discard them and contact a Whole Foods store about a refund. Anyone who has taken them and develops symptoms should seek advice from a health care provider.
Vitality Works can be reached at (505) 268-9950 during its stated weekday business hours. The supplied report does not give a deadline for refunds or name a scheduled update. Consumers should consult the FDA’s recall announcement or contact the company for current information about the affected lot and any subsequent notices.
Key Questions
Which ashwagandha capsules are included in the recall?
The recall covers one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules, in a 120-count white plastic bottle. The identifiers are lot 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 advises consumers to throw them away rather than return them. The source report says customers can request a refund at any Whole Foods store.
What symptoms should consumers watch for?
The FDA announcement lists fever, diarrhea, nausea, vomiting and abdominal pain as possible Salmonella symptoms. It says people who have taken the capsules and develop symptoms should contact a health care provider.
Have any illnesses been reported?
The source report said no illnesses linked to the recall had been reported at the time of publication. The supplied material does not provide a later update or confirm whether the investigation has concluded.
Where can I ask questions about the recall?
Vitality Works lists (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
