Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties
Recalled by A New Life Herbs, LLC
Food recall
A New Life Herbs, LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
A New Life Herbs, LLC has recalled Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 31, 2025 and was initiated on November 20, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, with approximately 275 bottles affected. The company behind the recall is A New Life Herbs, LLC, based in Somerville, TN. The FDA describes the product as: “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”
Why was Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties recalled?
According to the FDA, the stated reason for the recall is: “Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label.” In plain terms, this recall relates to an unapproved substance or additive.
This type of recall involves an ingredient or additive — such as a color, preservative, or other substance — that is not approved for use in the food as sold under U.S. rules. It does not automatically mean the product is harmful, but it does mean it does not meet current food regulations.
What should you do?
If you think you may have bought Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, compare it against the product description and identifying codes (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) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact A New Life Herbs, LLC or your local health authority.
About this recall
This recall was distributed in TN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Who this recall affects
This recall matters to anyone who bought Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN.
What unapproved substance or additive actually means
This type of recall involves an ingredient or additive — such as a color, preservative, or other substance — that is not approved for use in the food as sold under U.S. rules. It does not automatically mean the product is harmful, but it does mean it does not meet current food regulations.
In this case, the concern applies specifically to Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties from A New Life Herbs, LLC — not to the wider category of products. Similar items from other brands aren't part of this recall.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: 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
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact A New Life Herbs, LLC or your local health department.
Full recall details
- Status
- Terminated
- Date reported
- December 31, 2025
- Recall started
- November 20, 2025
- Distributed in
- TN
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties recalled?+
According to the FDA: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0347-2026. Information last synced from the FDA on September 29, 2026.