Severity
Moderate
ModerateClass IIOngoing
FDA Food recall · Reported December 31, 2025
Anti-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 283162814429
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Compiled from official public sources by the editorial team.
Verify with FDA Food →
A New Life Herbs, LLC recalled Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expe… - a moderate-severity action.
Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expe… was recalled by A New Life Herbs, LLC in December 31, 2025. Reason: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label. Check the official notice for the remedy. Verify recall #H-0340-2026 with the FDA Food before acting.
The recall
A New Life Herbs, LLC issued this moderate-severity FDA Food recall-Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label.
- Moderate
- severity level
- Class II
- classification
- December 31, 2025
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-0340-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-0340-2026) was formally reported on December 31, 2025, with the manufacturer initiating the action on November 20, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. A New Life Herbs, LLC is listed as the recalling firm, operating out of Somerville, TN. Federal records list the affected scope as 116 bottles.
The documented reason for this recall is: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label Distribution data in the federal record shows the product reached: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
116 bottles
Related Recalls
6
1 from same agency
Product description
Anti-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 283162814429
Reason for recall
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | H-0340-2026 |
| Date reported | December 31, 2025 |
| Date initiated | November 20, 2025 |
| Recalling firm | A New Life Herbs, LLC |
| Firm location | Somerville, TN |
| Affected scope | 116 bottles |
| Distribution | AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-0340-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Anti-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 283162814429. Recalled by A New Life Herbs, LLC. Units affected: 116 bottles.
Why was this product recalled? ▼
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Which agency issued this recall? ▼
This recall was issued by the FDA Food on December 31, 2025. Severity: Moderate. Recall number: H-0340-2026.
Where was the recalled product distributed? ▼
Distribution: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-0340-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 31, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.