Class ITerminatedVoluntary: Firm initiated

Herbs Forever: food recall H-0404-2026

Herbs Forever of Los Angeles, CA recalled HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814… Reason: Potential undeclared allergen ingredient (Wheat). The FDA listed it as Class I in its Enforcement Report dated Jan 21, 2026; distribution: nationwide.

Record status as published: Terminated (terminated May 5, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
Product quantity
45 units
Reason for recall
Potential undeclared allergen ingredient (Wheat)
Codes, lots and dates on the package
Batch: 124-4 Expiration date: 1/2029
Distribution pattern
Product is sold primarily on-line nationwide.
Recalling firm
Herbs Forever, Los Angeles, CA
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmJan 6, 2026
Classified by the FDAJan 14, 2026
Published in the Enforcement ReportJan 21, 2026
TerminatedMay 5, 2026

Other products in the same recall event

The FDA groups related products under one recall event (event 98267).

  • H-0405-2026 — HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0404-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.