Home / Recalls / McDaniel Life-Line LLC / D-1111-2019

D-1111-2019 Class II Terminated

Recalled by McDaniel Life-Line LLC — Felt, OK

FDA drug recall D-1111-2019 was initiated by McDaniel Life-Line LLC on Feb 8, 2019 and is designated Class II. Reason for recall: Unapproved new drug The recall status is terminated (terminated Dec 15, 2020). Affected quantity: 150 vials.

Recall details

Product Type: Drugs
Report Date: Apr 17, 2019
Initiation Date: Feb 8, 2019
Termination Date: Dec 15, 2020
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 150 vials

Product description

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

Reason for recall

Unapproved new drug

Distribution pattern

Nationwide, Italy, Australia, Canada, Poland

Code information

All lots within expiry

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1111-2019
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.