HIGH

A New Life Herbs Recalls Boswellia Herbal Supplement Over Labeling Issues

A New Life Herbs, LLC recalled 278 bottles of Boswellia Herbal Supplement on November 20, 2025. The product has unapproved drug claims and lacks a Supplement Facts label. Consumers should stop using it immediately and seek a refund.

Quick Facts at a Glance

Recall Date
November 20, 2025
Hazard Level
HIGH
Brand
A New Life Herbs
Category
Health & Personal Care
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 Boswellia Herbal Supplement packaged in a 2 oz. glass dropper bottle. The UPC code is 284260392420. It was distributed in several states, including Alabama, Arizona, and California.

The Hazard

The product features unapproved drug claims on its labeling and lacks a Supplement Facts label, which can mislead consumers about its contents and effects. These issues classify the recall as Class II, indicating a moderate to high risk.

Reported Incidents

There have been no reported incidents or injuries associated with this recall. Consumers are advised to discontinue use as a precaution.

What to Do

Consumers should stop using the Boswellia Herbal Supplement immediately. Contact A New Life Herbs, LLC for refund or replacement information via email.

Contact Information

For more information, consumers can reach A New Life Herbs, LLC at their website or email address provided in the recall notification.

Key Facts

  • Product UPC: 284260392420
  • Recalled quantity: 278 bottles
  • Distributed in AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
  • Class II recall due to labeling issues
  • Immediate stop-use advisory

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Safety Assessment

Risk LevelHIGH
Severity Score
6/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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