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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.

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Low RiskFDA Food
Food & Beverages/Dietary Supplements

Eclectic Herb Vitamin Herb Blend Recalled for Incorrect Labeling

Agency Publication Date: January 15, 2025
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Summary

Eclectic Institute Inc. has voluntarily recalled 1,334 bottles of Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement (750mg, 150 capsules) because of errors on the Supplement Facts panel. The product labels misstate ingredient quantities and list the wrong botanical names for Cayenne Root and Ginger Fruit. No illnesses or injuries have been reported to date.

Risk

The product label incorrectly identifies botanical names and lists inaccurate quantities for several ingredients. This could lead consumers to ingest different herbal components or amounts than they expect.

What You Should Do

  1. This recall affects Eclectic Herb Vitamin Herb Blend vita biotic dietary supplements sold in plastic bottles containing 150 capsules (750mg) with UPC 0 23363 52002 2.
  2. Check the label for lot number 25183 (Expiration Date 10/2024) or lot number 25543 (Expiration Date 03/2025) to see if your product is affected.
  3. Return the product to the place of purchase for a refund, throw it away, or contact Eclectic Institute Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions.

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: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement (750mg, 150 capsules)
Variants: 750mg, 150 capsules
UPC Codes:
023363520022
Lot Numbers:
25183 (Exp 10/2024)
25543 (Exp 03/2025)
GTIN:
023363520022

Affected label declared Oregon Grape 190mg and 97mg; Cayenne Root as Allium sativum (garlic) 195mg; and Ginger Fruit as Capsicum annuum (cayenne) 65mg.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96000
Status: Resolved
Manufacturer: Eclectic Institute Inc
Manufactured In: United States
Units Affected: 1334 bottles
Distributed To: Nationwide

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 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.