Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Food
Food & Beverages/Dietary Supplements

Herbs Forever Gastro Care and Hingwastika Churna Recalled for Undeclared Wheat

Agency Publication Date: January 14, 2026
Share:
Sign in to monitor this recall

Summary

Herbs Forever is voluntarily recalling 45 units of Gastro Care and Hingwastika Churna Ayurvedic herbal supplements because they may contain undeclared wheat. People who have an allergy or severe sensitivity to wheat run the risk of a serious or life-threatening allergic reaction if they consume these products. Both products are sold in 90-capsule containers and were distributed nationwide primarily through online sales. You should return the product to the place of purchase for a full refund or dispose of it immediately.

Risk

The supplements contain wheat that is not listed on the product label. This poses a critical risk to consumers with wheat allergies or celiac disease, as consumption could trigger a severe allergic response.

What You Should Do

  1. Check your supplement containers for Gastro Care (UPC 8 07814 00124 3) with Batch 124-4 and an expiration date of 1/2029.
  2. Check your supplement containers for Hingwastika Churna (UPC 8 07814 00622 4) with Batch 622-2 and an expiration date of 6/2029.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: HerbsForever- Gastro Care; Ayruvedic Herbal Supplement (90 VEGE Capsules)by Herbs Forever
Variants: Extract 800 MG each capsule
UPC Codes:
807814001243
Lot Numbers:
124-4 (Exp 1/2029)

Recall #: H-0404-2026

Product: HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement (90 VEGE Capsules)by Herbs Forever
Variants: 100 GMS
UPC Codes:
807814006224
Lot Numbers:
622-2 (Exp 6/2029)

Recall #: H-0405-2026

Product Images

Front of bottle, HerbsForever Gastro Care

Front of bottle, HerbsForever Gastro Care

Ingredient Label on bottle, HerbsForever Gastro Care

Ingredient Label on bottle, HerbsForever Gastro Care

Caution Label on bottle, HerbsForever Gastro Care

Caution Label on bottle, HerbsForever Gastro Care

Entire label, HerbsForever Gastro Care

Entire label, HerbsForever Gastro Care

Entire label, HerbsForever Hingwastika Churna

Entire label, HerbsForever Hingwastika Churna

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98267
Status: Resolved
Manufacturer: Herbs Forever
Sold By: online
Manufactured In: United States
Units Affected: 2 products (45 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. 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. Refer to the openFDA terms of service for more information.