HIGH

A New Life Herbs Recalls Sinus Cap Herbal Supplement Over Misbranding

A New Life Herbs recalled Sinus Cap Herbal Supplement on November 20, 2025, due to unapproved drug claims. The product lacks a Supplement Facts label, which misbrands it. Consumers should not consume the product and seek refunds or replacements.

Quick Facts at a Glance

Recall Date
November 20, 2025
Hazard Level
HIGH
Brand
A New Life Herbs
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

Hazard Information

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

What You Should Do

Consumers who have purchased this product should not consume it. Contact A New Life Herbs, LLC for refund or replacement information. Notification method: E-Mail

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Product Details

The Sinus Cap Herbal Supplement contains Fenugreek, Thyme, Oregon Grape Root, and Bentonite Clay. Each capsule weighs 510 mg, and the product is packaged in a plastic bag. The recall affects 38 bags distributed across Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Missouri, Mississippi, North Carolina, New York, and Tennessee.

The Hazard

The product is misbranded due to the absence of a Supplement Facts label. It also makes unapproved drug claims, which can mislead consumers about its intended effects.

Reported Incidents

No injuries or incidents have been reported related to this recall. The recall is classified as Class II by the FDA.

What to Do

Consumers should stop using the Sinus Cap Herbal Supplement immediately. Contact A New Life Herbs, LLC for refund or replacement information via email.

Contact Information

For questions or concerns about the recall, consumers can reach A New Life Herbs, LLC via email. More information is available at the FDA's recall page.

Key Facts

  • Recall date: November 20, 2025
  • 38 bags affected
  • Distributed in 12 states
  • No reported injuries
  • Unapproved drug claims on labeling

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
POISONING

Product Classification

Product Details

Model Numbers
C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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