Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Food
Food & Beverages/Dietary Supplements

A New Life Herbs Supplements Recalled for Unapproved Drug Claims

Agency Publication Date: December 23, 2025
Share:
Sign in to monitor this recall

Summary

A New Life Herbs, LLC is recalling 993 units of various herbal supplements, including Anti-virus, Baby Allergy, Baby Soothe, Boswellia, Chaga Mushroom, Ear Drops, Organic Ginger Root, Pain Away, and Sinus Cap products. These products are being recalled because they make unapproved drug claims on their labels and are missing the required Supplement Facts panel. Consumers should not use these products as they have not been evaluated for safety or effectiveness for the conditions listed on the labels.

Risk

The products are misbranded and marketed with claims that they can treat, cure, or prevent specific diseases, such as viral replication, cancer, and infections, without FDA approval. Using unproven treatments can delay necessary medical care from a healthcare professional.

What You Should Do

  1. Check your supplement packaging for the following product names: Anti-virus, Baby Allergy, Baby Soothe, Boswellia, Chaga Mushroom, Ear Drops, Organic Ginger Root, Pain Away, or Sinus Cap Herbal Supplements.
  2. Identify if your product is affected by matching the UPC codes (such as 283162814429, 249953949282, 284260392420, 284588087831, or 231946534537) and expiration dates ranging from 2025 to 2030. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a refund, throw it away, or contact A New Life Herbs, LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Anti-virus Herbal Supplement (2 oz.)
Variants: 1:5 Alcohol Tincture
UPC Codes:
283162814429
Lot Numbers:
T801AV (EXP 9/30)
T686AV (EXP 12/29)
T636AV (EXP 9/29)
T564AV (EXP 9/28)

Recall #: H-0340-2026; Contains: Forsethia blossoms, Sumac berries, Pine needles

Product: Baby Allergy Herbal Supplement (2 oz.)
Variants: Vegetable glycerin
UPC Codes:
249953949282
Lot Numbers:
E166SA (EXP 4/28)

Recall #: H-0341-2026

Product: Baby Soothe Herbal Supplement (2 oz.)
Lot Numbers:
E164BS (EXP 1/27)
E128BS (EXP 7/26)

Recall #: H-0342-2026

Product: Boswellia Herbal Supplement (2 oz.)
Variants: 1:5 Alcohol Double Extract
UPC Codes:
284260392420
Lot 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)

Recall #: H-0343-2026

Product: Chaga Mushroom Herbal Supplement (2 oz.)
Variants: 1:5 Alcohol Double Extract
UPC Codes:
284588087831
Lot Numbers:
T720CH (EXP 3/30)
T656CH (EXP 10/29)
T618CH (EXP 7/29)
T568CH (EXP 1/29)
T532CH (EXP 10/28)

Recall #: H-0344-2026

Product: Ear Drops Herbal Supplement (0.5 oz.)
Variants: Mullein flower alcohol tincture 1:5
Lot Numbers:
T553MF (EXP 12/28)

Recall #: H-0345-2026; Packaged in plastic dropper bottle

Product: Organic Ginger Root Herbal Supplement (50 capsules/560 mg)
Variants: Capsules
Lot Numbers:
C132GR (EXP 7/27)
C131GR (EXP 6/27)
C121GR (EXP 2/27)
C115GR (EXP 12/26)
C108GR (EXP 1/26)
C93GR (EXP 7/25)

Recall #: H-0346-2026; Packaged in a plastic bag

Product: Pain Away Herbal Supplement (4.5 oz. or 9 oz.)
Variants: Vegetable glycerin
UPC Codes:
231946534537
Lot Numbers:
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)

Recall #: H-0347-2026

Product: Sinus Cap Herbal Supplement (50 capsules/510 mg)
Variants: Capsules
Lot Numbers:
C136SC (EXP 10/27)
C128SC (EXP 5/27)
C110SC (EXP 9/26)
C109SC (EXP 4/26)
C102SC (EXP 10/25)

Recall #: H-0348-2026; Packaged in a plastic bag

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98037
Status: Active
Manufacturer: A New Life Herbs, LLC
Sold By: A New Life Herbs, LLC
Manufactured In: United States
Units Affected: 9 products (116 bottles; 23 bottles; 49 bottles; 278 bottles; 144 bottles; 22 bottles; 48 bags; 275 bottles; 38 bags)
Distributed To: Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Missouri, Mississippi, North Carolina, New York, Tennessee

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.