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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About This Product

Boswellia Herbal Supplement is derived from frankincense and is marketed for its anti-inflammatory properties. Consumers typically purchase it for relief from pain and inflammation.

Why This Is Dangerous

The product's unapproved drug claims and lack of a Supplement Facts label can mislead consumers about its efficacy and safety. This can lead to improper usage and potential health risks.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers should avoid using the product and seek refunds. The lack of proper labeling can lead to confusion and misinformed health decisions.

Practical Guidance

How to identify if yours is affected

  1. Check the UPC code on the bottle: 284260392420.
  2. Look for the model numbers: T848B EXP 11/30, T836B EXP 10/30, etc.
  3. Verify if you purchased the product between the specified dates.

Where to find product info

You can find the UPC code and model numbers on the product packaging, typically near the barcode or on the label.

What timeline to expect

Expect a refund processing time of approximately 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Keep a record of your communication attempts.
  • Contact relevant consumer protection agencies.
  • Consider escalating the issue through social media.

How to prevent similar issues

  • Always check for Supplement Facts labels on dietary supplements.
  • Research the brand and product claims online before purchase.
  • Look for products with third-party testing certifications.

Documentation advice

Document any correspondence with the manufacturer, keep receipts of purchase, and take photos of the product for your records.

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.

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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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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