HIGH

A New Life Herbs Recalls Pain Away Herbal Supplement Over Misbranding

A New Life Herbs recalled 275 bottles of Pain Away Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume this product and seek refunds.

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 Pain Away Herbal Supplement comes in 4.5 oz. and 9 oz. glass bottles. It contains Wood Betony and White Willow in vegetable glycerin. The product has UPC 231946534537.

The Hazard

The product has unapproved drug claims on its label and is misbranded due to the absence of a Supplement Facts label. This misbranding can mislead consumers about the product's safety and effectiveness.

Reported Incidents

No injuries or adverse effects related to the product have been reported. The recall addresses labeling issues rather than direct health risks.

What to Do

Consumers should stop using the Pain Away Herbal Supplement immediately. Contact A New Life Herbs at the provided email for refund or replacement information.

Contact Information

For more information, consumers can visit the FDA's recall report at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0347-2026.

Key Facts

  • Recall date: November 20, 2025
  • Active recall status
  • 275 bottles recalled
  • Distributed in AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

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Safety Assessment

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

Product Classification

Product Details

Model Numbers
E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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