a new life herbs, llcfoodHigh PriorityActive

Pain 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 231946534537

Pain 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 231946534537 was recalled because unapproved drug claims on product labeling and product misbranded due to no supplement facts label. If you have this product, stop using it until you verify your lot or model details.

By RecallRadar Editorial Team

Sourced from FDA. Last verified April 15, 2026.

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Key facts

Date announced: December 31, 2025
Source agency: FDA

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.

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

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand: A new life herbs, llc
Category: food
Source agency: FDA
Announced: December 31, 2025
Country: US
Status: Active

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25

#	Model
1	E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25

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

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

1Stop using the affected product until you verify whether your item is impacted.
2Check the official recall notice and match your model, lot, or serial details.
3Follow the official instructions for repair, replacement, refund, or disposal.

Open Official Recall Notice

Source & Verification

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

Official source: FDA
Announced by source: December 31, 2025
Last reviewed by RecallRadar: April 15, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the a new life herbs, llc recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/food/enforcement.json?search=recall_number:H-0347-2026&limit=1

Keep browsing with these internal hubs: a new life herbs, llc recall hub and Food & Drug recall hub.