TL;DR
Get workout gear delivered free with Prime
- Fast, free delivery on millions of items
- Prime Video, Amazon Music and more included
- Member-only deals all year
Vitality Works Inc. is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules because of potential Salmonella contamination. The FDA-posted company announcement says no illnesses have been reported; customers should not consume the product and can seek a refund at Whole Foods Market.
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, according to a company announcement posted by the U.S. Food and Drug Administration on October 30, 2026. The capsules were sold nationwide, and the announcement said no illnesses had been reported at the time.
The recall covers 120-count white plastic bottles bearing the 365 Whole Foods Market label. The affected lot number is 2025-26227, and the expiration date is 10/13/2028. Both identifiers are printed on the bottom of the bottle; the product UPC is 9948252099. Consumers should compare the details on their bottle with the recall information rather than relying on the brand name alone.
The capsules were available for purchase from November 24, 2025, through October 20, 2026, online through Amazon.com and in Whole Foods Market stores nationwide. The company said the potential contamination was identified through routine sampling of a single retail unit. That finding prompted the recall; the announcement does not say that every bottle in the lot was tested or contaminated.
Vitality Works advises customers who have the recalled capsules to stop using them and discard them. The company says consumers should not return the product to the store. Refunds are available 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.
How to Identify the Recalled Bottles
The recall matters because Salmonella can cause illness, and consumers may still have the capsules at home after purchasing them during the nearly 11-month sales period. Checking the lot number and expiration date helps distinguish the affected product from other 365-branded supplements that are not identified in this notice.
The FDA-posted announcement describes possible symptoms including fever, diarrhea, nausea, vomiting and abdominal pain. It says infection can be serious, and sometimes fatal, for young children, older or frail people, and people with weakened immune systems. In rare cases, the company notice says, infection may spread to the bloodstream and lead to more serious conditions. These are risks associated with Salmonella generally; the announcement does not report that any recalled capsule caused an infection.
For shoppers, the immediate action is specific: do not consume the affected lot, discard it and seek a refund at Whole Foods Market. The absence of reported illnesses is the status given in the announcement, not a guarantee that no exposure occurred or that the product is safe to use.
Products Worth Considering
Therabody Theragun Relief Massage Gun, 3-Speed, Navy
Oral-B iO Series 9 Limited Rechargeable Electric Toothbrush with 7 Cleaning Modes
Oura Ring 5 Smart Ring, Silver, Size 7
As an affiliate, we earn on qualifying purchases.
Recall Scope and Distribution Update
The FDA page labels the notice a company announcement and says it posts company recall notices as a public service; it does not endorse the product or company. The recall notice identifies Vitality Works, based in Albuquerque, New Mexico, as the recalling firm and gives potential Salmonella contamination as the reason.
The company announcement carries a dated clarification: it was updated on October 30, 2026 to reflect nationwide distribution rather than sales in selected states. The stated sales channels were Whole Foods Market stores across the country and Amazon.com. The product description is Standardized + Full Spectrum Blend Ashwagandha Capsules, 120 count.
The scope described is limited to one identified lot, number 2025-26227. The notice does not announce a recall of all ashwagandha products, all supplements sold at Whole Foods, or other lots of this product. Consumers should use the printed lot and expiration details to determine whether a bottle falls within the recall.
““No illnesses have been reported to date.””
— Vitality Works Inc., in the company announcement posted by the FDA
What the Notice Does Not Establish
The announcement says the potential contamination was found through routine sampling of one retail unit, but it does not identify where that unit was sampled, explain the test results in further detail, or state how many bottles from the lot may have been affected. It also does not say whether additional testing has been completed.
No illnesses had been reported when the company announcement was issued, according to the notice. It provides no later case updates and does not describe whether the firm or public health authorities are conducting further investigation. The notice also gives no information about how many bottles were sold or how many remain in consumers’ possession.
The published recall identifies one lot only. It does not clarify whether any other lots were assessed, or whether the contamination source has been determined. Those details are not established by the information provided in the notice.
Consumer Steps and Company Contact
Consumers can check the bottle bottom for lot 2025-26227 and expiration date 10/13/2028, alongside the UPC 9948252099 and 120-count product description. Anyone with a matching bottle should not take the capsules, should discard them and can request a refund at any Whole Foods Market store. The company says not to return the recalled product to the store.
People with questions about the recall can call Vitality Works at (505) 268-9950 during weekday business hours, 8 a.m. to 5 p.m. Mountain Time. The FDA-posted notice provides no date for a further update. Consumers seeking the latest status can check the FDA recall page or contact the company directly.
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, lot 2025-26227, with expiration date 10/13/2028 and UPC 9948252099.
Why were the capsules recalled?
Vitality Works said the lot has the potential to be contaminated with Salmonella. The company reported that the concern was identified through routine sampling of a single retail unit.
Have illnesses been reported?
The October 30, 2026, company announcement posted by the FDA said no illnesses had been reported to date. The notice does not provide a later illness update.
What should I do if I have a recalled bottle?
Do not consume it. Vitality Works says to discard the product rather than return it to the store. Refunds are available at any Whole Foods Market store.
Where can I ask questions about the recall?
Contact Vitality Works at (505) 268-9950, Monday through Friday, 8 a.m. to 5 p.m. Mountain Time.
Source: fda.gov
