Class ITerminatedVoluntary: Firm initiated
Herbs Forever: food recall H-0405-2026
Herbs Forever of Los Angeles, CA recalled HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4. 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- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
- Product quantity
- 45 units
- Reason for recall
- Potential undeclared allergen ingredient (Wheat)
- Codes, lots and dates on the package
- Batch: 622-2 Expiration date: 6/2029
- 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
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 6, 2026 |
| Classified by the FDA | Jan 14, 2026 |
| Published in the Enforcement Report | Jan 21, 2026 |
| Terminated | May 5, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 98267).
- H-0404-2026 — HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0405-2026 (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.