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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 capsules matching lot 2025-26227; the company says to discard them, and Whole Foods stores can provide refunds.
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 sampling found possible Salmonella contamination. Manufacturer Vitality Works Inc. says the capsules were sold nationwide through Whole Foods stores and Amazon.com; consumers with the identified lot should stop taking them and discard the product.
The recall covers 120-count white plastic bottles with 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. The announcement identifies Albuquerque-based Vitality Works Inc. as the company recalling the product.
According to the company announcement published by the FDA, routine sampling found that the capsules may be contaminated with Salmonella. The source says the product was distributed at Whole Foods stores and on Amazon.com from November 24, 2025, through October 20, 2026. It reports that no illnesses linked to the recall had been reported at the time of publication.
Consumers are instructed to stop using and throw away the capsules rather than return them. The announcement says customers can obtain a refund at any Whole Foods store. People who have taken the product and develop symptoms should contact a health care provider. Questions can be directed to Vitality Works at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Health Risks and Consumer Actions
The recall matters because Salmonella infection can range from gastrointestinal illness to severe complications, and some groups face a higher risk of serious disease. The FDA-published announcement warns that young children, older or frail people, and people with weakened immune systems may be particularly vulnerable. It also says that, in rare cases, infection can enter the bloodstream and lead to more serious conditions.
Consumers may have bought the capsules as a supplement and may not recognize that a product kept at home is part of a recall. Checking the lot number and expiration date against the notice can help identify the affected bottles. The source reports no linked illnesses so far, but that status does not establish that every bottle is free of risk or rule out later reports.
The notice lists symptoms including fever, diarrhea, nausea, vomiting, and abdominal pain; diarrhea may be bloody. Anyone who took the recalled capsules and develops symptoms is advised to contact a health care provider. The report does not provide individualized medical advice, and consumers with health concerns should consult a qualified clinician.
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How the Recall Was Identified
The development is a company recall announced through an FDA notice, rather than a report of confirmed illnesses. The stated reason was a potential contamination finding during routine sampling. The notice identifies one lot, not every ashwagandha product or every bottle sold under the 365 Whole Foods Market label.
The source gives a nationwide sales period running from November 2025 to October 2026 and names Whole Foods stores and Amazon.com as sales channels. That period is presented as reported in the recall coverage; readers should use the product identifiers in the notice to check a bottle, rather than assuming all capsules purchased during that period are affected.
“The organism can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.”
— FDA-published company announcement
What Is Not Yet Confirmed
The source reports no illnesses linked to the recall at the time of publication. It does not say whether any consumers have since reported illness, how many bottles were distributed, or how many may remain in homes or on sale. The reported test finding is described as possible contamination; the supplied material does not provide laboratory details or explain whether contamination was confirmed in finished products.
The source also does not state whether Amazon listings or store inventory have been fully removed, or whether further lots are being investigated. The sales dates and recall announcement date are reproduced as given in the material; the notice’s precise current status and any later updates are not established here.
Checking Bottles and Seeking Help
Consumers should compare the bottle’s bottom label with the recall identifiers: lot 2025-26227, UPC 9948252099, and expiration date 10/13/2028. If all identifiers match, do not take the capsules. Discard them as directed; Whole Foods stores are listed as the place to request a refund. The company’s phone line is available during the stated weekday business hours for questions.
Anyone who has taken the capsules and develops symptoms named in the notice should contact a health care provider. The recall source does not describe a deadline for refunds or provide details on additional testing or investigation. Consumers can check the FDA announcement and company updates for any later information about the affected lot, illness reports, or changes to the recall instructions.
Key Questions
Which ashwagandha capsules are included in the recall?
The recall covers 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules in 120-count bottles with lot number 2025-26227, UPC 9948252099, and expiration date 10/13/2028.
What should I do if I have a matching bottle?
Do not take the capsules. The company announcement says to throw them away rather than return them. Whole Foods stores can provide a refund, according to the recall coverage.
What symptoms should consumers watch for?
The notice lists fever, diarrhea, nausea, vomiting, and abdominal pain; diarrhea may be bloody. Contact a health care provider if symptoms develop after taking the product.
Have any illnesses been reported?
The source says no illnesses linked to the recall had been reported at the time of publication. It does not establish whether that status has changed since then.
Who can answer questions about the recall?
Vitality Works Inc. lists (505) 268-9950 for questions, Monday through Friday, from 8 a.m. to 5 p.m. Mountain Time.
Source: goodhousekeeping.com
