Lower riskFood recall · FDA · Published January 6, 2026
Herbs Forever Gastro Care Capsules Recall: Wheat Allergen Risk
Herbs Forever recalls 90-capsule Gastro Care herbal supplement due to potential undeclared wheat allergen. Consumers should check UPC 8 07814 00124 3 and batch 124-4 for affected products.
📍Recalling firmHerbs Forever501 S Harvard Blvd Apt 2 · Los Angeles, CA 90020-3513
✎ GovInfoNow plain-language explainer
Herbs Forever is recalling its Gastro Care herbal supplement capsules because they may contain undeclared wheat, which could cause allergic reactions in sensitive individuals. This recall affects products sold with the specific UPC and batch number. Read more at govinfonow.com/recall/6839-herbs-forever-gastro-care-capsules-recall-wheat-allergen-risk.
“Herbs Forever Gastro Care Capsules Recall: Wheat Allergen Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6839-herbs-forever-gastro-care-capsules-recall-wheat-allergen-risk. Based on FDA recall #H-0404-2026.
The FDA announced on Jan. 6, 2026, that Herbs Forever voluntarily recalled HerbsForever- Gastro Care Ayurvedic Herbal Supplement due to potential undeclared wheat allergen. Owners should contact the company for a refund. The recall involves 45 units sold primarily online nationwide.
UPC: 8 07814 00124 3 (also listed as 00807814001243)
Batch: 124-4
Expiration date: 1/2029
The hazard
The product contains a potential undeclared allergen ingredient, wheat. The FDA classified the recall as Class I.
Context
GovInfoNow's records show other recent recalls of similar products include Dreamland Zaatar Chickpea Salad Recall (2026-02-25), Vital Nutrients Aller-C Recall (2026-03-27), and Nuts.com Espresso Malted Milk Balls Recall (2026-03-10).
How to tell if you have this one
Check for the UPC code 8 07814 00124 3 and batch number 124-4 on the product packaging. The product is a 90-capsule herbal supplement labeled 'Gastro Care' with 800 mg per capsule.
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-0404-2026 (January 6, 2026)
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.