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FDA source record Class III Terminated

Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham,...

Recall Date: 2022-08-03 Recalling Firm: Eclectic Institute Inc Record Ref: F-0401-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham,... and names Eclectic Institute Inc as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Eclectic Institute Inc
  • Classification: Class III
  • Status: Terminated
  • Recall date: 2022-08-03
Best identifiers to check for a FDA record

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Product Description & Identification

Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham, OR 97030. The affected label declared "Oregon Grape 190mg ***Oregon Grape 97mg***Cayenne Root (Allium sativum) 195mg ***Ginger Fruit (Capsicum annuum) 65mg***".

Reason for Recall / Hazard Identified

Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Facts panel.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
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  5. Open the official FDA source below and follow its current instructions.

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Consumer Action Recorded in the Source

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Distribution & Affected States

nationwide

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0401-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
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