Vitality Works Inc. Recalls 365 Whole Foods Market Ashwagandha Capsules Sold Nationwide Due To Potential Salmonella Contamination
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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 product was sold nationwide at Whole Foods Market and online through Amazon; no illnesses had been reported as of the FDA notice dated October 30, 2026.

Vitality Works Inc. is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because the product may be contaminated with Salmonella, according to a company announcement posted by the U.S. Food and Drug Administration on October 30, 2026. The capsules were sold nationwide at Whole Foods Market stores and online through Amazon, and the company reported no illnesses as of the announcement.

The recall covers the 120-count white plastic bottle bearing UPC 9948252099, lot number 2025-26227, and expiration date 10/13/2028. The lot number and expiration date are printed on the bottom of the bottle. The company said the affected 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 says the recall applies to one lot. It does not state that other lots or other 365 products are included. The FDA posted the company’s announcement as a public service and says such postings do not constitute an endorsement of the product or company.

Customers who have a bottle matching the recalled lot should not consume it. The company says to discard it and not return it to a store. Refunds are available at any Whole Foods Market store. Consumers with questions can call Vitality Works at (505) 268-9950, Monday through Friday, from 8 a.m. to 5 p.m. Mountain Time.

At a glance
announcementWhen: Company announcement and FDA publicatio…
The developmentVitality Works recalled a single lot of 365 Whole Foods Market ashwagandha capsules after routine sampling identified potential Salmonella contamination.

Checking Bottles and Seeking Refunds

The recall concerns a product sold through two widely used retail channels, Whole Foods Market stores nationwide and Amazon. The sales period extended across nearly a year, so people who bought the capsules earlier may still have a bottle at home. Checking the lot number and expiration date—not just the product name—helps determine whether a bottle is covered.

Salmonella can cause illness, and the company’s notice describes young children, older or frail people, and people with weakened immune systems as being at greater risk of serious infection. For consumers, the immediate steps are to stop using the product if its identifying details match, discard it, and contact a Whole Foods Market store about a refund. The recall notice does not say that illness has occurred, and it does not establish that any particular bottle is contaminated.

The announcement also illustrates why lot information matters in a product recall: the stated scope is one identified lot, not every ashwagandha supplement under the 365 name. Consumers should compare the printed identifiers with the recall details rather than infer coverage from the brand or product category alone.

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How the Recall Was Identified

The FDA page is dated October 30, 2026, the same date as the company announcement. It describes the issue as a potential Salmonella contamination and says the company identified it through routine sampling of one retail unit. The source material does not give further details about the sample, where it was collected, or the testing process.

The company announcement included a correction dated October 30: it was updated to reflect nationwide distribution, rather than sales in selected states. The product had been sold both through Amazon.com and at Whole Foods Market stores between November 24, 2025, and October 20, 2026. That distribution update is relevant to customers checking whether the recall could apply to a purchase made outside a limited region.

The FDA describes its role in posting company announcements as providing a public service. Its notice says the agency does not endorse the product or company. The recall information therefore reflects the company’s announcement as published by the FDA, rather than an FDA statement endorsing the product.

““No illnesses have been reported to date.””

— Vitality Works Inc., in its recall announcement

Scope and Illness Reports

The notice identifies one lot and says no illnesses had been reported when the company issued its announcement. It does not describe how many bottles were made or sold, how many remain in circulation, or whether further testing has confirmed contamination beyond the single retail unit referenced in the notice. The stated risk is potential contamination; the announcement does not say that every bottle in the recalled lot contains Salmonella.

It is also not clear from the provided material whether additional lots or products are being investigated, whether any later illness reports have emerged, or whether the company or regulators will issue further updates. The information reflects the status described in the FDA-posted announcement on October 30, 2026.

Consumer Steps and Company Contact

Consumers can compare a bottle’s label and bottom markings with the recall identifiers: UPC 9948252099, lot 2025-26227, and expiration date 10/13/2028. If all relevant details match, the company advises against consuming the capsules, says to discard them rather than return them, and directs customers to seek a refund at any Whole Foods Market store.

Questions can be directed to Vitality Works at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time. The FDA notice does not give a date for any follow-up update or describe a separate investigation milestone. Consumers should consult the company or FDA recall page for any later information about the affected lot or illness reports.

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, from lot 2025-26227. The listed UPC is 9948252099, and the expiration date is 10/13/2028.

Where and when was the recalled product sold?

According to the company announcement, the capsules were 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 bottle from the recalled lot?

Do not consume it. Vitality Works says to discard the product and not return it to the store. Refunds are available at any Whole Foods Market location.

Have any illnesses been reported?

The company said no illnesses had been reported as of its October 30, 2026, announcement. The notice does not establish whether later reports have been made.

Who can answer questions about the recall?

Vitality Works lists (505) 268-9950 for consumer questions. The company says its phone line is available Monday through Friday, from 8 a.m. to 5 p.m. Mountain Time.

Source: fda.gov

Wellness content on this site is informational and not a substitute for professional medical guidance.
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