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Vitality Works Inc. recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because of potential Salmonella contamination. The capsules were sold nationwide at Whole Foods Market and online through Amazon; no illnesses had been reported as of the October 30, 2026 announcement.
Vitality Works Inc. has recalled one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules over potential Salmonella contamination, according to a company announcement posted by the U.S. Food and Drug Administration on October 30, 2026. The 120-count bottles were sold nationwide at Whole Foods Market stores and through Amazon; the company said no illnesses had been reported at the time of the announcement.
The recall covers bottles identified by lot number 2025-26227 and expiration date 10/13/2028, both printed on the bottom of the bottle. The product is packaged in a white plastic bottle labeled 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha, 120 count, with UPC 9948252099. The company said the capsules were available for purchase from November 24, 2025, through October 20, 2026.
Vitality Works said the potential contamination was identified through routine sampling of a single retail unit. The company’s announcement says the recall concerns one lot. It does not report confirmed contamination in every bottle from that lot, and the FDA posting describes the issue as a potential risk. No illnesses had been reported when the notice was published.
People who have the identified product should not consume it. The company advises customers to discard it rather than return it to a store. Refunds are available at any Whole Foods Market location. Consumers with questions can call Vitality Works at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
How to Identify the Recalled Bottles
The recall matters to people who bought this supplement during the stated sales period because Salmonella can cause foodborne illness, and the product was distributed through retail stores and an online marketplace across the country. Checking the lot and expiration information on the bottle can help distinguish the recalled product from other ashwagandha products or other lots of the same brand.
The FDA announcement says Salmonella infection may cause fever, diarrhea, nausea, vomiting and abdominal pain. Diarrhea may be bloody. The notice warns that young children, older or frail people, and people with weakened immune systems can be at greater risk of serious illness. In rare cases, it says, infection can enter the bloodstream and lead to more severe conditions, including arterial infections, endocarditis or arthritis.
The recall is a precaution based on the potential for contamination, not a report that consumers have become ill. The company reported no illnesses to date. Customers should follow the recall instructions even if they feel well, and anyone with health concerns after consuming the capsules can contact a health professional.
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Nationwide Distribution and Recall Notice
The FDA page identifies the notice as a company announcement and says it posts company recall and safety notices as a public service. The agency states that posting an announcement does not mean it endorses the company or product. The recall was announced by Vitality Works, which is based in Albuquerque, New Mexico.
The FDA posting includes a distribution correction: the company’s press release was updated on October 30 to say the product had been distributed nationwide, rather than in selected states. The stated sales channels were Whole Foods Market stores and Amazon.com. That correction is relevant for consumers checking where the product was available, but the notice does not list individual stores or provide a count of bottles sold.
The notice is specific to the 120-count capsules in lot 2025-26227. It does not say that other lots, product sizes, or other ashwagandha products are included. Consumers should compare the information printed on the bottle with the recall identifiers before deciding whether their product is covered.
“The product has the potential to be contaminated with Salmonella.”
— Vitality Works Inc., in its recall announcement
What the Contamination Notice Establishes
The notice says potential Salmonella contamination was identified during routine sampling of a single retail unit, but it does not provide test results, explain whether the organism was confirmed in that unit, or say how the contamination may have occurred. It also does not state how many bottles from the lot were distributed or whether any were recovered.
No illnesses had been reported as of the company announcement, but the notice does not provide later updates or a final investigation outcome. It is also unclear from the notice whether additional testing has been conducted beyond the routine sample, or whether other lots are under review. The recall notice applies to the identified lot and does not announce a broader product recall.
Check the Lot and Follow Recall Steps
Consumers who have the 120-count bottles should check the label and the bottom of the container for lot 2025-26227 and expiration date 10/13/2028. If both identify the recalled product, the company says not to take the capsules, to discard them, and not to return them to a store. Customers can request a refund at any Whole Foods Market store.
People seeking more information can contact Vitality Works at (505) 268-9950 during its stated weekday business hours, 8 a.m. to 5 p.m. Mountain Time. Consumers who have consumed the capsules and are concerned about symptoms can seek advice from a health professional. The announcement does not give a date for a further update; any new information about testing, illnesses or the scope of the recall would depend on subsequent company or FDA notices.
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, from lot 2025-26227. The UPC is 9948252099, and the listed expiration date is 10/13/2028.
Where and when were the capsules sold?
Vitality Works said the product was sold from November 24, 2025, through October 20, 2026, at Whole Foods Market stores nationwide and online through Amazon.com.
What should I do if I have a recalled bottle?
Do not consume the capsules. The company advises customers to discard the product and not return it to a store. Refunds are available at any Whole Foods Market location.
Have any illnesses been reported?
Vitality Works said no illnesses had been reported when it issued the recall announcement on October 30, 2026. The notice does not establish whether any later reports were made.
Why was the product recalled?
The company said routine sampling of a single retail unit identified a potential Salmonella contamination risk. The announcement does not provide further testing details or say that every bottle in the recalled lot was contaminated.
Source: fda.gov
