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Sundial Herbal Products Lawsuit

Sundial is recalling dozens of unapproved herbal products which are misbranded and may be dangerous because their safety and efficacy have not been established, according to the U.S. Food & Drug Administration (FDA).

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If you or a loved one was injured, you should contact our law firm immediately. You may be entitled to compensation by filing a Sundial Herbal Products Lawsuit and we can help. Please click the button below for a Free Confidential Case Evaluation or call us toll-free 24 hrs/day by dialing (866) 588-0600.

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What’s the Problem?

According to the FDA Recall Notice, this action affects the following Sundial Herbal Products:

  • Tenadam Herb
  • Spiced Tea
  • Nigerian Moringa Leaf Powder
  • Jamaican Turmeric
  • Bitter Wood
  • Devil Horsewhip
  • Mango Leaf
  • Red Water Grass
  • Sarsaparilla
  • Marsh Marigold
  • Sea Moss/Irish Moss
  • Dog Blood
  • Guava Leaf
  • Jack in the Bush
  • King of the Forest
  • ETHIOPIAN ABISH (FENNUGREEK SEED PWD.)
  • Ethiopian Traditional Talba (Flaxseed Meal Cereal)
  • Fever Grass
  • Jamaican Milk Wiss
  • Spanish Needle
  • Fig Leaf
  • Diabetics
  • Flax Seed Oil & Honey Blend
  • Bitter Kola (Arogbo)
  • Jamaican Bissy Powder
  • Ghanian Black Spice
  • Piss A Bed
  • White Pond Lily
  • Purple Sage
  • Quassia Wood
  • Trumpet Leaf
  • White Jointa
  • White Sage
  • Guinea Hen Weed
  • Sundial Cassava Meal
  • Cocoa Balls
  • African Fever Bush
  • Mojo Bush
  • Blood Leaf
  • Wood & Root Tonic
  • Koromantee
  • Ashanti
  • African Manback Tonic
  • Pimento
  • Mitmitta (Cayenne Pepper)
  • Mahogany Bark
  • Chaney Root
  • Cerasee Bay Leaves, Mango Bark
  • Asthma
  • Blood Pressure
  • Heart
  • Worms and Parasites
  • Flu-Allergies /HayFever
  • Arthritis
  • Axum Traditional Ethiopian Honey Beverage
  • Black Sage
  • Black Wiss
  • Cinnamon
  • Palo De Brazil
  • Broom Weed
  • Bread Nut
  • Jamaican and Tropical Raw Honey
  • Hemp Seed Oil
  • Talibah’s Tooth Powder and Ethiopian Coffe
  • Blue Vervain

These products were distributed from January 1, 2014, through July 2020, and contain labeling
“making drug claims stating the product(s) can diagnose, cure, mitigate, treat or prevent disease,” FDA said.

The recalled supplements are misbranded and are considered unapproved drugs based on labeling claims which could result in a delay of appropriate treatment by a healthcare provider. Because these products are unapproved, their safety and efficacy have not been established.

All supplements affected by the recall can be identified by the “Sundial” label with brown glass bottles, boxes, Ziploc bags and paper bags with clear viewing windows. The products were distributed via Internet sales or Sundial store pick up at 3609 Boston Road, Bronx, New York.

If you purchased any Sundial Herb Products that are affected by this recall, you should stop using them immediately. Anyone concerned about an adverse reaction to dietary supplements should consult their healthcare provider immediately.

Do I Have a Sundial Herbal Products Lawsuit?

The Pharmaceutical Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in Sundial Herbal Products Lawsuits. We are handling individual litigation nationwide and currently accepting new injury and death cases in all 50 states.

If you or a loved one was injured after taking a Sundial Herbal Product, you should contact our law firm immediately. You may be entitled to a settlement by filing a suit and we can help.

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