HIGH

A New Life Herbs Recalls Herbal Supplement Over Misbranding Issues

A New Life Herbs, LLC recalled 116 bottles of its anti-virus herbal supplement on November 20, 2025. The product misbranded due to unapproved drug claims and missing Supplement Facts label. Consumers should stop using the product immediately 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 a 2 oz. alcohol tincture containing Forsethia blossoms, Sumac berries, and Pine needles. It has UPC number 283162814429. The product was distributed in multiple states including California, New York, and Georgia.

The Hazard

The product makes unapproved drug claims and lacks a required Supplement Facts label. These issues can mislead consumers about the product's safety and efficacy.

Reported Incidents

No injuries or adverse reactions have been reported in connection with this recall. The product's misbranding poses potential health risks.

What to Do

Consumers should not consume the product. To request a refund or replacement, contact A New Life Herbs, LLC via email.

Contact Information

For more information, consumers can visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0340-2026.

Key Facts

  • 116 bottles recalled
  • Contains Forsethia blossoms, Sumac berries, Pine needles
  • Distributed in AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
  • Consumers advised to stop use immediately

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
POISONING

Product Classification

Product Details

Model Numbers
T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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