RecallRadar
High RiskReported January 21, 2026

HerbsForever- Hingwastika Churna

Recalled by Herbs Forever

Food recall

Herbs Forever

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving an undeclared allergen

Herbs Forever has recalled HerbsForever- Hingwastika Churna, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on January 21, 2026 and was initiated on January 6, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers HerbsForever- Hingwastika Churna, with approximately 45 units affected. The company behind the recall is Herbs Forever, based in Los Angeles, CA. The FDA describes the product as: “HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4”

Why was HerbsForever- Hingwastika Churna recalled?

According to the FDA, the stated reason for the recall is: “Potential undeclared allergen ingredient (Wheat).” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought HerbsForever- Hingwastika Churna, compare it against the product description and identifying codes (Batch: 622-2 Expiration date: 6/2029) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Herbs Forever or your local health authority.

About this recall

This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
January 21, 2026
Recall started
January 6, 2026
Distributed in
CA
What was recalled
HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
Why it was recalled (as stated by the FDA)
Potential undeclared allergen ingredient (Wheat)
How to identify the affected product
Batch: 622-2 Expiration date: 6/2029
Amount recalled
45 units

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was HerbsForever- Hingwastika Churna recalled?+

According to the FDA: Potential undeclared allergen ingredient (Wheat)

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have HerbsForever- Hingwastika Churna?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0405-2026. Information last synced from the FDA on July 5, 2026.

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