A New Life Herbs, LLC

FDA Regulatory Profile

A New Life Herbs, LLC has 9 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "A New Life Herbs, LLC" and its spelling variant "A New Life Herbs".

Latest recall
H-0342-2026 · Class II · Nov 20, 2025
Latest inspection
Nov 4, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls9Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent recalls

9 recall records on Nov 20, 2025.

NumberClassProductDate
H-0342-2026Class IIBaby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething…Nov 20, 2025
H-0344-2026Class IIChaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with…Nov 20, 2025
H-0340-2026Class IIAnti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant…Nov 20, 2025
H-0345-2026Class IIEar Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic…Nov 20, 2025
H-0346-2026Class IIOrganic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases…Nov 20, 2025
H-0348-2026Class IISinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient…Nov 20, 2025
H-0347-2026Class IIPain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in…Nov 20, 2025
H-0341-2026Class IIBaby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock…Nov 20, 2025
H-0343-2026Class IIBoswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful…Nov 20, 2025

Recent FDA inspections

1 inspection on Nov 4, 2025.

DateSiteProductClassificationFEI
Nov 4, 2025Somerville, TNFood/CosmeticsVoluntary Action Indicated (VAI)3040509817
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3040509817Somerville, TN1Nov 4, 2025

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.