HIGHFDA FOOD

A New Life Herbs Recalls Herbal Supplement Over Misbranding Issues

A New Life Herbs, LLC recalled 116 bottles of its anti-virus herbal supplement on November 20, 2025. The product misbranded due to unapproved drug claims and missing Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

Official notice
A New Life HerbsFood & BeveragesT801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA FOOD
Recall date
November 20, 2025
Status
ACTIVE
Severity
7/10

Quick Facts at a Glance

Recall Date
November 20, 2025
Hazard Level
HIGH
Brand
A New Life Herbs
Category
Food & Beverages
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
A New Life Herbs
Product type
Alcohol Tincture
Model numbers
T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
Sold at
Multiple Retailers
Where affected
Nationwide

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    November 20, 2025

  2. Reported by FDA FOOD

    December 31, 2025

  3. RecallRadar source check

    January 7, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

What You Should Do

Consumers who have purchased this product should not consume it. Contact A New Life Herbs, LLC for refund or replacement information. Notification method: E-Mail

About This Product

This herbal tincture is marketed for its alleged anti-viral properties and expectorant benefits. Consumers often purchase herbal supplements for immune support and respiratory health.

Why This Is Dangerous

The product's unapproved claims may lead consumers to believe it can treat or prevent viral infections, which is not substantiated. The absence of a Supplement Facts label means consumers cannot verify ingredients or dosages.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may face health risks if they rely on this product for serious health conditions. The recall creates an inconvenience for those who purchased it.

Practical Guidance

How to identify if yours is affected

  1. Check the UPC code on the product: 283162814429.
  2. Verify if your product matches the models listed in the recall.
  3. Inspect for the presence of a Supplement Facts label; if absent, the product is affected.

Where to find product info

The UPC code is typically located on the bottom of the bottle or on the packaging.

What timeline to expect

Expect a refund or replacement within 4-6 weeks after contacting the manufacturer.

If the manufacturer is unresponsive

  • Follow up with A New Life Herbs via email after two weeks.
  • Consider reporting the issue to the FDA if no response is received.

How to prevent similar issues

  • Look for supplements with clear Supplement Facts labels in the future.
  • Verify the product's claims against reputable sources before purchase.
  • Choose products certified by recognized health authorities.

Documentation advice

Document your purchase details, including dates, receipts, and any emails exchanged regarding the recall.

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Product Details

The recalled product is a 2 oz. alcohol tincture containing Forsethia blossoms, Sumac berries, and Pine needles. It has UPC number 283162814429. The product was distributed in multiple states including California, New York, and Georgia.

Key Facts

  • Contains Forsethia blossoms, Sumac berries, Pine needles
  • Distributed in AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
  • Consumers advised to stop use immediately

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
POISONING

Product Classification

Product Details

Model Numbers
T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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