CLASS II Drug recall · Reported 17 Apr 2019 · FDA Enforcement Report

Life-Line tm Catalytic Activated Energy Water container recalled

McDaniel Life-Line is recalling Life-Line tm Catalytic Activated Energy Water container, McDaniel Life-Line LLC 1775 US, distributed nationwide in the US. The recall was initiated on 8 Feb 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots within expiry.
Quantity recalledUnknown

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1112-2019
FDA event ID
82106
Recalling firm
McDaniel Life-Line, Felt, OK
Classification
Class II
Status
Terminated
Recall initiated
8 Feb 2019
FDA classified
9 Apr 2019
Reported
17 Apr 2019
Type
Voluntary: Firm initiated
Customers notified by
Press Release

Timeline

8 Feb 2019Recall initiated by company
9 Apr 2019Classified by FDA+60 days
17 Apr 2019Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Unapproved new drug

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

Life-Line tm Catalytic Activated Energy Water, 1 gallon container, McDaniel Life-Line LLC 1775 US Hwy 385 806-647-1741 Dimmitt, TX 79027

Where it was distributed

Nationwide, Italy, Australia, Canada, Poland

Nationwide

Questions about this recall

Is Life-Line tm Catalytic Activated Energy Water container, McDaniel Life-Line LLC 1775 US recalled?

Yes. McDaniel Life-Line recalled Life-Line tm Catalytic Activated Energy Water container, McDaniel Life-Line LLC 1775 US on 8 Feb 2019. The recall is Class II and its status is Terminated. Recall number D-1112-2019.

Why was it recalled?

Unapproved new drug

Which lots are affected?

All lots within expiry.

Where was it sold?

Nationwide, Italy, Australia, Canada, Poland

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from McDaniel Life-Line

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DrugCLASS IIIndian Herb Paste (a dietary supplement) Ingredients recalledMcDaniel Life-LineHidden Drug IngredientsNationwide