McDaniel Life-Line LLC recalls Indian Herb Paste (a dietary supplement) Ingredients: Galangal, Indian Paint, Yellow Dock & Licorice in an alloy of
McDaniel Life-Line recalls Indian Herb Paste dietary supplement containing unapproved ingredients. This product poses a drug safety risk and should not be used.
Stop using this now
Unapproved new drug
Contact the company & request your remedy
What happened, in plain English
McDaniel Life-Line is recalling Indian Herb Paste dietary supplements that contain unapproved ingredients. This recall is due to the product being classified as an unapproved new drug, which poses a safety risk. Read more at govinfonow.com/recall/39199-mcdaniel-life-line-indian-herb-paste-dietary-supplement-recall-unapproved.
Source Summary by GovInfoNow · govinfonow.com/recall/39199-mcdaniel-life-line-indian-herb-paste-dietary-supplement-recall-unapproved · Updated October 5, 2026 · FDA enforcement record: FDA #D-1111-2019
Cite this page
“McDaniel Life-Line Indian Herb Paste Dietary Supplement Recall: Unapproved Drug Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39199-mcdaniel-life-line-indian-herb-paste-dietary-supplement-recall-unapproved. Based on FDA recall #D-1111-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1111-2019%22&limit=1).
Why it’s dangerous
The product contains unapproved ingredients that are classified as a new drug. This means the product has not been approved by the FDA for safety and effectiveness, potentially causing health risks.
Who’s affected
People who own or use Indian Herb Paste dietary supplements from McDaniel Life-Line LLC in Dimmitt, TX. Those most at risk are individuals who have consumed the product without knowing it was unapproved.
How to tell if you have this one
Look for Indian Herb Paste dietary supplements with ingredients including Galangal, Indian Paint, Yellow Dock, and Licorice in alloy form. The product was sold by McDaniel Life-Line LLC in Dimmitt, TX and includes Zinc Chloride in 6 dram vials.
- Brand
McDaniel Life-Line- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Nationwide, Italy, Australia, Canada, Poland
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1111-2019 | Indian Herb Paste (a dietary supplement) Ingredients: Galangal, Indian Paint, Yellow Dock & Licorice in an alloy of Life-Line tm and Zinc Chloride in 6 dram vials, McDaniel Life-Line LLC, Dimmitt, TX; All lots within expiry | 150 vials |
| D-1112-2019 | Life-Line tm Catalytic Activated Energy Water, 1 gallon container, McDaniel Life-Line LLC 1775 US Hwy 385 806-647-1741 Dimmitt, TX 79027; All lots within expiry. | Unknown |
What to do — step by step
Stop Using Now
Immediately stop using the recalled Indian Herb Paste dietary supplement as it contains unapproved ingredients classified as a new drug.
Questions people ask
Is this product safe to use?
No, this product contains unapproved ingredients classified as a new drug and is not safe for use.
What should I do if I have this product?
You should stop using it immediately and contact McDaniel Life-Line LLC for further instructions.
How can I check if I have the recalled product?
Look for Indian Herb Paste dietary supplements with ingredients including Galangal, Indian Paint, Yellow Dock, and Licorice in alloy form sold by McDaniel Life-Line LLC in Dimmitt, TX.
Contact McDaniel Life-Line
We’ve drafted a message you can send McDaniel Life-Line to request your refund or repair — edit it as you like.
Subject: Recall D-1111-2019 — McDaniel Life-Line McDaniel Life-Line Hello, I own a McDaniel Life-Line that is covered by recall D-1111-2019 from McDaniel Life-Line. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1111-2019 (February 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1111-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.