A New Life Herbs — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, A New Life Herbs has 9 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 20 Nov 2025. A New Life Herbs is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for A New Life Herbs
How serious are A New Life Herbs recalls?
FDA recall classifications by severity
Full FDA recall history for A New Life Herbs
All 9 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 20 Nov 2025Official FDA Notice | Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 cap | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properti | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thym | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: F | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory pro | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
| 20 Nov 2025Official FDA Notice | Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Gi | Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label | Class IIOngoing |
Where have A New Life Herbs recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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