HIGH

A New Life Herbs Recalls Organic Ginger Root Supplement Over Misbranding

A New Life Herbs recalled 48 bags of Organic Ginger Root Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume the product and seek a refund.

Quick Facts at a Glance

Recall Date
November 20, 2025
Hazard Level
HIGH
Brand
A New Life Herbs
Category
Food & Beverages
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

Hazard Information

Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

What You Should Do

Consumers who have purchased this product should not consume it. Contact A New Life Herbs, LLC for refund or replacement information. Notification method: E-Mail

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Product Details

The recalled product is Organic Ginger Root Herbal Supplement, available in 50 capsules of 560 mg each. It was distributed in Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Missouri, Mississippi, North Carolina, New York, and Tennessee.

The Hazard

The supplement has unapproved drug claims on its labeling, which misleads consumers about its intended use. Additionally, it does not include a Supplement Facts label, violating labeling regulations.

Reported Incidents

No injuries or adverse effects have been reported concerning this recall. The FDA classified the issue as a Class II recall, indicating a potential health hazard.

What to Do

Consumers should stop using the product immediately. Contact A New Life Herbs, LLC via email to arrange for a refund or replacement.

Contact Information

For more information, email A New Life Herbs, LLC. Visit the FDA website for recall details at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0346-2026.

Key Facts

  • Recalled product: Organic Ginger Root Herbal Supplement
  • Quantity: 48 bags
  • Recall date: November 20, 2025
  • Distribution states: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
  • Contact via email for refund

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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