FDA recall H-0347-2026 · Dec 31, 2025
A New Life Herbs, LLC: Pain Away Herbal Supplement recall
Product
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
Reason for recall
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Terminated
- Codes, lots and dates
- 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
- 275 bottles
- Distribution
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Recalling firm
- A New Life Herbs, LLC, Somerville, TN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-11-20
Source: openFDA enforcement record H-0347-2026 · search recall number H-0347-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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