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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- A New Life Herbs
- Product type
- Boswellia Herbal Supplement
- 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
- Sold at
- Multiple Retailers
- Where affected
- Nationwide
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 20, 2025
Reported by FDA FOOD
December 31, 2025
RecallRadar source check
January 7, 2026
Consumer action
Use the official remedy and keep documentation.
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
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
- Check the UPC code on the bottle: 284260392420.
- Look for the model numbers: T848B EXP 11/30, T836B EXP 10/30, etc.
- 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.
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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.
Key Facts
- 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 Guide
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