CLASS III Food recall · Reported 22 Jan 2025 · FDA Enforcement Report
Eclectic Herb Vitamin Herb Blend vita biotic dietary recalled
Eclectic Institute is recalling Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg per, distributed nationwide in the US. The recall was initiated on 3 Aug 2022 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0401-2025
- FDA event ID
- 96000
- Recalling firm
- Eclectic Institute, Gresham, OR
- Brand
- Eclectic Herb
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 3 Aug 2022
- FDA classified
- 15 Jan 2025
- Reported
- 22 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Foreign Material
- Product category
- Vitamins
Timeline
| 3 Aug 2022 | Recall initiated by company | |
| 15 Jan 2025 | Classified by FDA | +896 days |
| 22 Jan 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
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***".
Where it was distributed
nationwide
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
Lot 25183; Exp date 10/2024 Lot 25543; Exp Date 03/2025
Where was it sold?
nationwide
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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