RecallHawk
Class II Recall

Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory pro

A New Life Herbs, LLC

Summary

The FDA issued a Class II for Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankinc by A New Life Herbs, LLC. Reason: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label.

Details

Source

Food Recall

External ID

H-0343-2026

Action Date

2025-12-31

Status

Ongoing

Category

food

Product Description

Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420

Lot/Code Info: 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

Quantity Affected: 278 bottles

Reason for Recall

Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

Distribution

AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

Type: Voluntary: Firm initiated

Recall Initiated: 2025-11-20

Company

A New Life Herbs, LLC

Somerville, TN

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.

A New Life Herbs, LLC has 9 FDA actions in our database, including 9 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (A New Life Herbs, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does A New Life Herbs, LLC have FDA actions?

A New Life Herbs, LLC has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0343-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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