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Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because routine testing found potential Salmonella contamination. The FDA announcement identifies lot 2025-26227, sold at Whole Foods stores and Amazon; no illnesses linked to the recall had been reported in the source report.
The U.S. Food and Drug Administration published a recall announcement dated October 30 after Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because routine testing found potential Salmonella contamination. The affected lot was sold through Whole Foods stores and Amazon, and consumers are advised not to take it.
The recall covers capsules in a 120-count white plastic bottle with lot number 2025-26227, UPC 9948252099, and expiration date 10/13/2028. The report says the lot number and expiration date are printed on the bottom of the bottle. Consumers should compare all identifying details, rather than relying on the product name alone, to determine whether a bottle is affected.
The product was distributed nationwide at Whole Foods stores and on Amazon.com. The source report gives the sale period as November 24, 2025, through October 20, 2026; its summary also describes distribution from November 2025 through October 2026. The date range is reported as stated, but the materials do not explain the apparent timing relative to the October 30 announcement.
Vitality Works said the recall followed routine sampling in which the capsules may have tested positive for Salmonella. No illnesses linked to the recall had been reported in the source report. Consumers who have the identified lot should not use it and should discard the capsules rather than return them. The company announcement says customers can seek a refund at any Whole Foods store.
The Health Risks of Salmonella Exposure
The recall matters because Salmonella infection can cause gastrointestinal illness and may become severe, particularly for young children, older or frail people, and people with weakened immune systems. The FDA announcement says healthy people who become infected can experience fever, diarrhea that may be bloody, nausea, vomiting, and abdominal pain.
The agency also warned that, in rare cases, the bacteria can enter the bloodstream and lead to more serious conditions. That risk is not a claim that contaminated capsules have caused illness in this instance: the report said no related illnesses had been reported at the time. The recall is a precaution tied to possible contamination, and consumers should act on the lot information even if they feel well.
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How the Recalled Lot Was Identified
The affected product is an ashwagandha supplement sold under the 365 Whole Foods Market label and manufactured by Vitality Works Inc., based in Albuquerque, New Mexico. According to the FDA-published company announcement, the recall applies to one lot, not every ashwagandha product or every bottle of the named supplement.
The potential contamination was identified through routine sampling, according to the report. The recall notice names the product, lot number, UPC, and expiration date so customers can check the label. This information is more useful for identifying affected bottles than the product category or brand by itself.
Illness Reports and Distribution Dates
The source report said no illnesses linked to the recall had been reported, but it does not establish whether any cases could be identified later. The available information also does not say how many bottles were distributed, how many have been recovered, or whether testing found contamination in every capsule from the lot. The notice describes potential contamination, not proof that every bottle is contaminated.
The reported sales dates run from November 24, 2025, to October 20, 2026, while the FDA announcement is dated October 30. The source material does not clarify that timing, and it should not be taken as confirmation of a different date range. Consumers can use the lot number, UPC, and expiration date on their bottle to check whether it matches the recall.
Checking Bottles and Seeking Help
Consumers should stop taking capsules that match lot 2025-26227 and discard them, following the company announcement’s instructions not to return the product. A refund is available at any Whole Foods store, according to the report. Customers with questions can contact Vitality Works Inc. at (505) 268-9950, Monday through Friday, from 8 a.m. to 5 p.m. Mountain Time.
Anyone who has taken the capsules and develops fever, diarrhea, nausea, vomiting, or abdominal pain should contact a health care provider promptly, as advised in the announcement. The source material does not give a separate deadline for refunds or say how further updates will be issued, so consumers should check directly with Whole Foods or Vitality Works for current assistance.
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 bottle, lot 2025-26227, UPC 9948252099, with expiration date 10/13/2028.
Where were the recalled capsules sold?
The source report says the affected lot was sold at Whole Foods stores and Amazon.com. It describes distribution nationwide.
What should I do with a bottle from the recalled lot?
Do not take the capsules. The company announcement says to throw them away rather than return them. The report says customers can obtain a refund at any Whole Foods store.
What symptoms should I watch for after taking the capsules?
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 product.
Have illnesses been reported?
The source report said no illnesses linked to the recall had been reported at the time it was published. That status could change, and the report does not provide later updates.
Source: goodhousekeeping.com
