HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
Summary
The FDA issued a Class I for HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules by Herbs Forever. Reason: Potential undeclared allergen ingredient (Wheat).
Details
Source
Food Recall
External ID
H-0405-2026
Action Date
2026-01-21
Status
Terminated
Category
food
Product Description
HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
Lot/Code Info: Batch: 622-2 Expiration date: 6/2029
Quantity Affected: 45 units
Reason for Recall
Potential undeclared allergen ingredient (Wheat)
Distribution
Product is sold primarily on-line nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-06
Company
Los Angeles, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Herbs Forever has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Herbs Forever) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Herbs Forever have FDA actions?
Herbs Forever has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0405-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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