Ear Drops Herbal Supplement recall

Recalled by A New Life Herbs, LLC · Somerville, TN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle

Quantity: 22 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

T553MF EXP 12/28

Where it was sold

Alabama Arizona California Georgia Illinois Indiana Minnesota Missouri Mississippi North Carolina New York Tennessee

FDA's distribution note: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: A New Life Herbs, LLC
Initiated by: Voluntary: Firm initiated
Recall initiated: Nov 20, 2025
In FDA report of: Dec 31, 2025
Terminated: Aug 28, 2026
FDA recall number: H-0345-2026 · event 98037
Official record: FDA enforcement report search

Also recalled with it (8 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Labeling Nov 20, 2025