RecallHawk
Class II Recall

Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin,

A New Life Herbs, LLC

Summary

The FDA issued a Class II for Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Beto 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-0347-2026

Action Date

2025-12-31

Status

Ongoing

Category

food

Product Description

Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537

Lot/Code Info: E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25

Quantity Affected: 275 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-0347-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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