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Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules after routine sampling found possible Salmonella contamination. Consumers should not take the capsules; the company says to discard them, and Whole Foods stores will provide refunds.
The U.S. Food and Drug Administration published a recall announcement dated October 30 for one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules after routine sampling found possible Salmonella contamination. Vitality Works Inc., the Albuquerque, New Mexico, company named in the announcement, says consumers should stop using the capsules and throw them away; no illnesses linked to the recall had been reported in the source material.
The recall covers lot 2025-26227 of the supplement, sold in a 120-count white plastic bottle. The UPC is 9948252099, and the expiration date is 10/13/2028. The company announcement says the lot number and expiration date are printed on the bottom of the bottle, where consumers can check whether their product is affected.
The reported sales period is November 24, 2025, through October 20, 2026, at Whole Foods Market stores nationwide and through Amazon.com. The source describes the product as distributed nationwide and says the concern arose from routine sampling. It does not say that every bottle was contaminated; the stated basis for the recall is that the capsules may contain Salmonella.
Consumers with the affected lot are advised not to take the capsules and to discard them rather than return them. The company announcement says customers can obtain a refund at any Whole Foods store. People who have taken the supplement and develop symptoms should contact a health care provider, according to the recall guidance.
Risks for Supplement Users
The recall matters because Salmonella infection can cause fever, diarrhea, nausea, vomiting and abdominal pain, and illness can be more serious for young children, older or frail people, and people with weakened immune systems. The FDA announcement warns that, in rare cases, the bacteria can enter the bloodstream and lead to more severe infections.
Unlike a food product that may be consumed quickly, a bottle of supplements can remain in a household and be taken over time. Checking the lot number and expiration date helps consumers distinguish the recalled product from other ashwagandha capsules. The recall is limited to the specified lot in the supplied information; it does not identify all products containing ashwagandha as affected.
The announcement reported no linked illnesses at the time covered by the source. That status is not proof that no one has become ill; it reflects the information reported when the notice was issued. Consumers who feel unwell after taking the product should seek medical advice rather than assume symptoms are unrelated.
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How the Recall Was Identified
The FDA published a company announcement on October 30, naming Vitality Works Inc. as the recalling firm. The notice says the possible contamination was identified through routine sampling. The supplied report does not describe the testing method, the number of samples, or whether contamination was confirmed in individual consumer bottles.
The affected capsules are sold under the 365 Whole Foods Market label, with sales reported at Whole Foods stores and Amazon.com. The company named in the notice is Vitality Works Inc. of Albuquerque, New Mexico. The recall information provided is specific to one lot and includes a refund option through Whole Foods stores.
What Testing Has Not Established
The source says routine sampling found that the capsules may be contaminated, but it does not provide test results or confirm that Salmonella was found in every bottle—or in any particular bottle sold to a consumer. It also gives no estimate of how many bottles from the affected lot remain in homes or in distribution.
The source reports no illnesses linked to the recall so far, but does not provide a later case count or say whether the investigation has concluded. It is also unclear from the supplied material whether additional lots or products are being examined. The reported sales dates and the October 30 announcement date are retained as given in the source; the material does not explain their timing or provide a later status update.
Checking Bottles and Getting Refunds
Consumers can compare the bottom of their bottle with the recall details: lot 2025-26227, UPC 9948252099, and expiration date 10/13/2028. Anyone with a matching bottle should not use it and should discard it, following the company’s instruction not to return the capsules. Whole Foods stores are listed as the place to request a refund.
For questions, the company announcement lists Vitality Works Inc. at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time. People who have taken the capsules and experience fever, diarrhea, nausea, vomiting, or abdominal pain should contact a health care provider. The source material provides no further investigation deadline or scheduled update.
Key Questions
Which ashwagandha capsules are included in the recall?
The recall covers lot 2025-26227 of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules. The product is in a 120-count white plastic bottle, with UPC 9948252099 and expiration date 10/13/2028.
Where can I find the lot number and expiration date?
The company announcement says both are printed on the bottom of the bottle. Check those details against the recall information before taking the supplement.
What should I do with a matching bottle?
Do not take the capsules. The company says to throw them away rather than return them. A refund is available at any Whole Foods store, according to the announcement.
What symptoms should I watch for?
The FDA announcement lists fever, diarrhea, nausea, vomiting and abdominal pain; diarrhea may be bloody. If you took the capsules and develop symptoms, contact a health care provider. The notice warns that young children, older or frail people, and people with weakened immune systems may be at higher risk of serious illness.
Have illnesses been reported?
The source report says no illnesses linked to the recall had been reported at the time of its account. It does not provide a later case count or say whether the investigation is complete.
Source: goodhousekeeping.com
