RecallHawk
Class III Recall

Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 520

Eclectic Institute Inc

Summary

The FDA issued a Class III for Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 caps by Eclectic Institute Inc. Reason: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Fact.

Details

Source

Food Recall

External ID

F-0401-2025

Action Date

2025-01-22

Status

Terminated

Category

food

Product Description

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***".

Lot/Code Info: Lot 25183; Exp date 10/2024 Lot 25543; Exp Date 03/2025

Quantity Affected: 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.

Distribution

nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-03

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Eclectic Institute Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Eclectic Institute Inc have FDA actions?

This is the only FDA action we have on record for Eclectic Institute Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0401-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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