Eclectic Herb Vitamin Blend Dietary Supplement Recalled for Label Errors
Eclectic Herb Vitamin Herb Blend dietary supplement is recalled because the Supplement Facts panel contains incorrect ingredient names and quantities. Consumers should check affected lot numbers.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class III recall involving a labeling error with no reported illnesses or injuries. The incorrect ingredient names and quantities on the Supplement Facts panel constitute a minor labeling issue, consistent with a Moderate severity score.
Plain-English summary
Eclectic Institute Inc is recalling its Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement (750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2). Approximately 1,334 bottles are affected, distributed nationwide.
The product's Supplement Facts panel contains ingredient names and quantities that are not listed correctly. This includes errors related to Oregon Grape, Cayenne Root, and Ginger Fruit, which may not match the actual product composition or intended amounts.
Consumers who have purchased this product should check if they have one of the affected lots: Lot 25183 (expiration 10/2024) or Lot 25543 (expiration 03/2025). Those with concerns about the listed ingredients or quantities should consult a healthcare provider.
The recalled product
- 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…
- Manufacturer
- Eclectic Institute Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,334
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot 25183
- Exp date 10/2024 Lot 25543
- Exp Date 03/2025
Distribution
Distributed nationwide across the United States.
Related recalls
Same hazard · mis labeling
See all →- SevereImperio Distribution Recalls Beef Jerky Produced Without Federal Inspection
USDA FSIS · 2026-10-24
- LowMagellan LeadCare II Blood Lead Test Kit Recall for Labeling Error
FDA (Devices) · 2026-10-21
- ModerateIn2bones Recalls Partially Threaded Bone Screws Due to Labeling Error
FDA (Devices) · 2026-10-21
- SevereInstrumentation Laboratory Recalls HemoslL AcuStar HIT-lgG In Vitro Diagnostic Reagents
FDA (Devices) · 2026-10-21
- SevereDeano's Pasta Recalls Pear and Pecorino Ravioli for Undeclared Lobster
FDA (Food) · 2026-10-21
Similar recalls
- LowNature's Blend Folic Acid Recalled for Labeling Error
FDA (Food) · 2020-04-08
- ModerateBaby Allergy herbal supplement recalled over unapproved drug claims and misbranding
FDA (Food) · 2025-12-31
- ModerateHealthmaxx Recalls Organic OPC69 Dietary Supplements Due to Mislabeling
FDA (Food) · 2013-10-02
- ModerateIowa Select Herbs Recalls Acia Berry Supplement Due to Misbranding
FDA (Food) · 2016-05-11
- ModerateOrganic ginger root capsules recalled over unapproved drug claims and misbranding
FDA (Food) · 2025-12-31
- ModerateHealthmaxx Recalls Organic Grapeseed Extract Due to Mislabeling
FDA (Food) · 2013-10-02