HerbsForever- Hingwastika Churna
Reason Potential undeclared allergen ingredient (Wheat)
HerbsForever- Gastro Care recall
Recalled by Herbs Forever · Los Angeles, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential undeclared allergen ingredient (Wheat)
Undeclared allergen: Wheat
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
Quantity: 45 units
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Batch: 124-4 Expiration date: 1/2029
Where it was sold
Nationwide.
FDA's distribution note: Product is sold primarily on-line nationwide.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Herbs Forever
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 6, 2026
- In FDA report of
- Jan 21, 2026
- Terminated
- May 5, 2026
- FDA recall number
- H-0404-2026 · event 98267
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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