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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 Recall Class Action 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) 223-3784.

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What’s the Problem?

This FDA Recall affects the following Sundial Herbal Products, which were distributed from January 1, 2014, through July 2020:

  • 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 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 herbs contain false labeling stating they can diagnose, cure, mitigate, treat or prevent disease, according to the FDA.

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

Affected herbal supplements are affixed with the “Sundial” label, and are packaged in brown glass bottles, boxes, Ziploc bags or paper bags with clear viewing windows. The products were sold online and at the Sundial store at 3609 Boston Road, Bronx, New York.

Consumers who purchased any recalled Sundial Herb Products should stop using them immediately and return them for a refund.

This recall was issued on July 9, 2020.


Do I Have a Sundial Herbal Products Recall Class Action 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 Recall Class Action 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.

FREE Confidential Case Evaluation

To contact us for a free review of your potential case, please fill out the form below or call us toll free 24 hrs/day by dialing: (866) 223-3784.

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