a new life herbs, llcfoodHigh PriorityActive

Baby 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 249953949282

a new life herbs, llc Baby 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 249953949282 was recalled by the FDA. Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: November 20, 2025
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## Baby 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 249953949282 Agency: FDA | Category: food | Date: 2025-11-20 Reason: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label What to do:
2Stop using the product if it matches your lot/model.
3Compare your product details with the FDA recall notice.
4Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Open Official Recall Notice Get Alerts for a new life herbs, llc Devices

What's Being Recalled

Quoted source excerpt from the official notice.

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

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

E166SA EXP 4/28

#	Model
1	E166SA EXP 4/28

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my a new life herbs, llc device affected?

Check the affected models section on this page. The official notice currently lists E166SA EXP 4/28.

What is the remedy for this recall?

## Baby 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 249953949282 Agency: FDA | Category: food | Date: 2025-11-20 Reason: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label What to do: 1. Stop using the product if it matches your lot/model. 2. Compare your product details with the FDA recall notice. 3. Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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