Herbs Forever food recall: HerbsForever- Gastro Care
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 98267
- Recall initiated
- Jan 6, 2026
- Classified by FDA
- Jan 14, 2026
- Posted in Enforcement Report
- Jan 21, 2026
- Terminated
- May 5, 2026
- Recalling firm
- Herbs Forever
- Firm location
- Los Angeles, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 2
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Potential undeclared allergen ingredient (Wheat)
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Jan 6, 2026. FDA classified it 8 days later, on Jan 14, 2026. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: Product is sold primarily on-line nationwide.
Recalled products (2)
H-0404-2026 Class I Terminated
HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
Codes / lots: Batch: 124-4 Expiration date: 1/2029
Quantity: 45 units
H-0405-2026 Class I Terminated
HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
Codes / lots: Batch: 622-2 Expiration date: 6/2029
Quantity: 45 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98267
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.