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Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because the product may be contaminated with Salmonella. The lot was sold nationwide at Whole Foods Market stores and through Amazon from November 24, 2025, to October 20, 2026; no illnesses had been reported as of the company announcement.
Vitality Works Inc. is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because the capsules may be contaminated with Salmonella, according to a company announcement posted by the U.S. Food and Drug Administration on October 30, 2026. The affected 120-count bottles were sold nationwide at Whole Foods Market stores and online through Amazon; no illnesses had been reported at the time of the notice.
The recall covers bottles bearing lot number 2025-26227 and an expiration date of 10/13/2028. Both identifiers are printed on the bottom of the white plastic bottle. The product label reads 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha, 120 count, and the UPC is 9948252099. The company said the product was available for purchase from November 24, 2025, through October 20, 2026.
Vitality Works, based in Albuquerque, New Mexico, said the potential contamination was identified through routine sampling of a single retail unit. The FDA notice names Salmonella as the reason for the recall, but does not say that contamination was confirmed in every bottle or provide further laboratory findings. The company announcement was updated on October 30 to clarify that distribution was nationwide, rather than limited to selected states.
Customers who have a bottle from the recalled lot should not consume it. The company says to discard the product rather than return it to a store. Customers can obtain a refund at any Whole Foods Market store or call Vitality Works at (505) 268-9950. The company lists its phone hours as Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
How the Recall Affects Shoppers
The recall concerns a supplement distributed through retail stores nationwide and Amazon, so customers may have purchased the product in different parts of the country and through more than one sales channel. Checking the lot and expiration information on the bottle is the practical way to determine whether a purchase is included; the notice does not call for discarding other lots of the product.
Salmonella can cause illness, and the FDA-posted company announcement says infections may be serious, particularly for young children, older or frail people, and people with weakened immune systems. Listed symptoms include fever, diarrhea, nausea, vomiting and abdominal pain. The notice also describes rare cases in which infection can affect the bloodstream and lead to more severe illness. These are general risks associated with Salmonella, not evidence that anyone became sick from this recalled product.
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Distribution and Recall Timeline
The company says the capsules were offered for sale for nearly 11 months, from November 24, 2025, through October 20, 2026. The announcement and FDA publication followed on October 30, 2026. Its update that day corrected the stated distribution scope to nationwide, replacing an earlier reference to sales in selected states.
The FDA page explains that it posts company announcements about recalls, market withdrawals and safety alerts as a public service. It also says the agency’s posting does not constitute an endorsement of the company or its product. The notice identifies one lot and says routine sampling of a single retail unit prompted the recall; it does not describe a broader finding across other products or lots.
“The firm press was updated on 10/30/2026 to reflect nationwide product distribution rather than to select states.”
— Vitality Works Inc., in the company announcement posted by the FDA
What the Notice Does Not Establish
The notice describes a potential for Salmonella contamination and says the recall followed routine sampling of a single retail unit. It does not provide test results, say whether Salmonella was confirmed in that unit, or explain how many bottles from the lot were distributed. It also does not identify the source of any possible contamination.
Although the company reported no illnesses to date, that status reflects information available when the announcement was published. The notice does not say whether additional testing or an investigation is underway, or whether the company or regulators have received reports since then.
Consumer Steps and Company Contact
Consumers can compare the bottle’s product name, 120-count size, lot number 2025-26227 and expiration date with the recall details. If the bottle matches, the company’s instruction is to stop using it and discard it; a refund is available at any Whole Foods Market store. The notice says not to return the recalled product to the store.
Customers with questions can contact Vitality Works at (505) 268-9950 during the listed weekday business hours. The FDA-posted notice does not give a date for a further update or describe additional action beyond the recall and refund instructions. Readers should rely on later notices from the company or FDA for any new information about the affected lot or reported illnesses.
Key Questions
Which ashwagandha capsules are included in the recall?
The recall covers 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules, 120 count, with UPC 9948252099, lot number 2025-26227 and expiration date 10/13/2028.
Where and when were the recalled capsules sold?
Vitality Works says the product was available nationwide at Whole Foods Market stores and through Amazon.com from November 24, 2025, through October 20, 2026.
What should I do if I have a bottle from the recalled lot?
Do not consume it. The company says to discard the product and not return it to the store. Refunds are available at any Whole Foods Market store.
Have any illnesses been reported?
The company reported no illnesses to date in its October 30, 2026 announcement. The notice does not establish whether reports may be received later.
Who can answer questions about the recall?
Vitality Works lists (505) 268-9950 for consumer questions. Its stated phone hours are Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Source: fda.gov
