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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.

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Medium RiskFDA Drug
Medications & Supplements/Dietary Supplements

McDaniel Life-Line LLC: Indian Herb Paste and Life-Line Water Recalled as Unapproved New Drugs

Agency Publication Date: April 9, 2019
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Summary

McDaniel Life-Line LLC is recalling 150 vials of Indian Herb Paste and all lots of Life-Line Catalytic Activated Energy Water. These products are being recalled because they are being marketed as unapproved new drugs without FDA safety and effectiveness evaluations. The Indian Herb Paste contains ingredients like Galangal, Indian Paint, Yellow Dock, and Licorice, while the Energy Water was sold in 1-gallon containers. Consumers should stop using these products and contact their healthcare provider.

Risk

These products have not been evaluated by the FDA for safety or effectiveness, which means their quality, purity, and therapeutic claims are unverified. Using unapproved drugs can lead to serious health risks if they contain harmful substances or if consumers rely on them instead of seeking proven medical treatments for health conditions.

What You Should Do

  1. Check your supply for Indian Herb Paste in 6 dram vials and Life-Line Catalytic Activated Energy Water in 1-gallon containers.
  2. Verify if your Indian Herb Paste is affected by checking the vial for ingredients like Galangal, Indian Paint, and Zinc Chloride; all lots within their expiry date are included in this recall.
  3. Identify the affected Life-Line Catalytic Activated Energy Water by looking for 1-gallon containers from McDaniel Life-Line LLC; all lots within their expiry date are included.
  4. Stop using these products immediately and contact your healthcare provider or pharmacist for guidance regarding your health.
  5. Return any unused product to the place of purchase for a refund and contact McDaniel Life-Line LLC at 806-647-1741 for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare consultation and product return

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Indian Herb Paste (6 dram vials)
Model:
D-1111-2019
Lot Numbers:
All lots within expiry
Product: Life-Line tm Catalytic Activated Energy Water (1 gallon container)
Model:
D-1112-2019
Lot Numbers:
All lots within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82106
Status: Resolved
Manufacturer: McDaniel Life-Line LLC
Manufactured In: United States
Units Affected: 2 products (150 vials; Unknown)
Distributed To: Nationwide

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.