HIGH

A New Life Herbs Recalls Chaga Mushroom Supplement Over Misbranding

A New Life Herbs, LLC recalled 144 bottles of Chaga Mushroom Herbal Supplement on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a 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 the Chaga Mushroom Herbal Supplement, packaged in a 2 oz. glass dropper bottle. It has a UPC of 284588087831 and was distributed in states including Alabama, California, and New York.

The Hazard

The product presents a high hazard level due to unapproved drug claims on its labeling. Additionally, it lacks a Supplement Facts label, which is essential for consumer safety.

Reported Incidents

No injuries or adverse events have been reported in connection with this recall. However, the misbranding raises concerns about consumer safety.

What to Do

Consumers should not consume the product. Contact A New Life Herbs, LLC via email for refund or replacement information.

Contact Information

For more details, consumers can visit the FDA's recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0344-2026.

Key Facts

  • Brand: A New Life Herbs
  • Model: Chaga Mushroom Herbal Supplement
  • Recall Date: November 20, 2025
  • Quantity: 144 bottles
  • Distribution: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

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Safety Assessment

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

Product Classification

Product Details

Model Numbers
T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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