FDA Alerts Consumers: Nationwide Recall Of Certain Ashwagandha Capsules 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 after routine testing found possible Salmonella contamination. The FDA said no illnesses linked to the recall had been reported; consumers should not take the capsules and should discard them.

The U.S. Food and Drug Administration published a recall notice on October 30 for one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules after routine testing found possible Salmonella contamination. Vitality Works Inc., the Albuquerque, New Mexico, company named in the notice, said consumers should not take the capsules and should discard them.

The recall covers capsules in a 120-count white plastic bottle bearing 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. Consumers should check those identifiers rather than relying on the product name alone.

The report says the product was sold at Whole Foods Market stores nationwide and through Amazon.com. It gives a distribution period of November 24, 2025, through October 20, 2026. Those dates extend beyond the reported October 30 announcement, and the available material does not explain the discrepancy. The timing should be treated as unclarified pending further information.

The company’s instructions are to throw the capsules away, not return them. Customers can seek a refund at any Whole Foods store. The report says no illnesses linked to the recall had been reported when the notice was published. People who have taken the capsules and develop symptoms should contact a health care provider, according to the recall information.

At a glance
updateWhen: Recall notice published October 30; the…
The developmentThe FDA published a company recall notice for one lot of Whole Foods Market ashwagandha capsules because routine testing found possible Salmonella contamination.

Check the Lot Before Taking Capsules

This recall concerns a supplement sold through a national grocery chain and a major online retailer, so people who bought ashwagandha capsules may need to inspect products already at home. Checking the lot, UPC, and expiration date can help determine whether a bottle is included; the recall applies to the specified lot, not automatically to every ashwagandha product or every 365-branded supplement.

Salmonella infection can be more serious for young children, older adults, frail people, and those with weakened immune systems. The FDA notice says healthy people can also develop illness, including fever, diarrhea, nausea, vomiting, and abdominal pain. The reported absence of linked illnesses is the status at the time of the notice, not a guarantee that exposure has not occurred.

Following the instruction not to use the capsules and to discard them reduces the risk of further exposure. Anyone with symptoms after taking the product should seek medical advice rather than assuming the symptoms are unrelated.

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How the Contamination Was Detected

According to the supplied report, the potential contamination was identified through routine sampling and testing. The FDA published a company announcement identifying Vitality Works Inc. as the recalling firm. The material does not describe the testing method, the number of samples, or whether contamination was confirmed in every bottle from the lot.

The recall notice identifies a single lot of the 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules. The listed package details are intended to help shoppers distinguish the affected product. The company’s consumer guidance is to discard the capsules and contact Whole Foods about a refund; questions can also be directed to Vitality Works at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.

“The organism can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.”

— FDA recall notice, as quoted in the report

Distribution Dates Need Clarification

The reported sale period runs from November 24, 2025, through October 20, 2026, while the FDA notice is dated October 30 and the source describes it as an announcement made on that date. The available information does not explain how sales could have continued through a date later than the notice. The distribution dates, as well as the exact timing of sales at individual stores and online, need confirmation.

The source says routine testing found the capsules may be contaminated; it does not establish that every bottle in the lot contains Salmonella. No linked illnesses had been reported at the time of the report, but the material does not provide later case updates, testing results beyond the initial finding, or details on how many bottles were distributed or recovered.

Follow Recall and Health Updates

Consumers should compare any bottle they own with the lot number, UPC, and expiration date in the recall notice. If it matches, they should not take the capsules and should discard them as instructed; Whole Foods stores can provide information about refunds. Consumers with questions can call Vitality Works during the listed weekday business hours.

Anyone who has taken the recalled capsules and develops symptoms associated with Salmonella should contact a health care provider. Further clarification of the distribution dates, along with any updates to illness reports or recall instructions, would help consumers understand the scope of the affected sales.

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 white plastic bottle, lot 2025-26227, UPC 9948252099, with expiration date 10/13/2028.

What should I do if I have the recalled bottle?

Do not take the capsules. The company says to throw them away rather than return them. Whole Foods stores can provide a refund.

What symptoms can Salmonella cause?

The FDA notice lists fever, diarrhea, nausea, vomiting, and abdominal pain; diarrhea may be bloody. The notice says infection can be more serious for young children, older adults, frail people, and people with weakened immune systems. Contact a health care provider if symptoms occur after taking the capsules.

Have any illnesses been linked to this recall?

The report said no illnesses linked to the recall had been reported when the notice was published. It does not provide a later illness update.

Where can I ask questions about the recall?

Vitality Works lists (505) 268-9950 for questions, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time. Whole Foods stores can address refund requests.

Source: goodhousekeeping.com

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