Class IIITerminatedVoluntary: Firm initiated
Eclectic Institute Inc: food recall F-0401-2025
Eclectic Institute Inc of Gresham, OR recalled Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363… Reason: 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. The FDA listed it as Class III in its Enforcement Report dated Jan 22, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Jan 15, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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***".
- Product quantity
- 1334 bottles
- Reason for recall
- 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.
- Codes, lots and dates on the package
- Lot 25183; Exp date 10/2024 Lot 25543; Exp Date 03/2025
- Distribution pattern
- nationwide
- Recalling firm
- Eclectic Institute Inc, Gresham, OR
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 3, 2022 |
| Classified by the FDA | Jan 15, 2025 |
| Published in the Enforcement Report | Jan 22, 2025 |
| Terminated | Jan 15, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0401-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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