Recall Register

Food recall: Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains…

Class II FDA enforcement event 98037. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

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

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

A New Life Herbs, LLC started this food recall on 20 Nov 2025. The firm address in the FDA record is in Somerville, TN. FDA put the recall in Class II. FDA event 98037 has 9 product records. The first FDA enforcement report date is 31 Dec 2025. The record gives the status Terminated, with the termination date 28 Aug 2026.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

Recalling firm

A New Life Herbs, LLC, Somerville, TN.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

9 product records in the event.

FDA event 98037: product records
Recall numberProductQuantityClassStatusReport date
H-0340-2026Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429116 bottlesClass IITerminated31 Dec 2025
H-0341-2026Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 24995394928223 bottlesClass IITerminated31 Dec 2025
H-0342-2026Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle49 bottlesClass IITerminated31 Dec 2025
H-0343-2026Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420278 bottlesClass IITerminated31 Dec 2025
H-0344-2026Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831144 bottlesClass IITerminated31 Dec 2025
H-0345-2026Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle22 bottlesClass IITerminated31 Dec 2025
H-0346-2026Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag48 bagsClass IITerminated31 Dec 2025
H-0347-2026Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537275 bottlesClass IITerminated31 Dec 2025
H-0348-2026Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag38 bagsClass IITerminated31 Dec 2025

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Food events that started in 2025
569
Share of these events in Class II
54%
Product records in this event
9
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 98037. https://recallregister.com/fda/ii/98037/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
What quantity of product is in FDA event 98037?
The event has 9 product records. The first record gives this quantity: 116 bottles
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2025 have the same class?
54% of the 569 food events that started in 2025 are in Class II.