• Mon - Fri: 8:00 - 18:00
Anvisa

Consumer Alert: Ervas Brasillis Supplements Suspended from Sale Due to Sanitary Irregularities

Discover why Ervas Brasillis natural products have been banned from circulation, with the focus on the lack of proper licensing.

The National Health Surveillance Agency (Anvisa), as a public health protection measure, announced on Friday, September 5, the prohibition of 32 dietary supplements produced by Ervas Brasillis Produtos Naturais Ltda. The agency’s decision, detailed in an official publication, requires the immediate seizure and full interdiction of all batches of the affected products.

The scope of the prohibition is comprehensive: Anvisa expressly bans the commercialization, distribution, manufacturing, importation, advertising, and use of any of these supplements. This strict action was triggered by serious irregularities uncovered during a sanitary inspection.

Understanding the Reasons Behind the Ervas Brasillis Ban

Anvisa’s inspection revealed that Ervas Brasillis was operating in a facility without the required sanitary license. In addition to the absence of proper authorization, the inspection uncovered unsanitary conditions and a complete lack of compliance with good food manufacturing practices—procedures that are essential to ensuring the safety and quality of consumer products.

List of Supplements Banned by Anvisa

For your safety and awareness, below is the list of dietary supplements from Ervas Brasillis and its associated brands that have been prohibited from commercialization, distribution, or use:

  • Creatine Monohydrate Red Fruit Flavor – Turbo Black Vitamin brand (all batches)
  • Creatine – Turbo Black Vitamin brand (all batches)
  • Type II Undenatured Collagen Yogurt Flavor – Turbo Black brand (all batches)
  • Hydrolyzed Collagen Tropical Fruit Flavor – Turbo Black Vitamin brand (all batches)
  • Caffeine with Taurine – Turbo Black Vitamin brand (all batches)
  • Moringa – Ervas Brasil brand (all batches)
  • Peruvian Maca – Ervas Brasil brand (all batches)
  • Hibiscus – Ervas Brasil brand (all batches)
  • Soursop – Ervas Brasil brand (all batches)
  • Tadala Natural – NB Nutrition brand (all batches)
  • Magnesium Threonate – Turbo Black Vitamin brand (all batches)
  • Peruvian Maca – Turbo Black Vitamin brand (all batches)
  • Black Maca – Turbo Black Vitamin brand (all batches)
  • Lactoze Gluten-Free – Turbo Black Vitamin brand (all batches)
  • L-Arginine and Alanica – Turbo Black Vitamin brand (all batches)
  • K2 + D3 2000 IU – Turbo Black Vitamin brand (all batches)
  • Energy Maca – Turbo Black Vitamin brand (all batches)
  • Creatine Monohydrate Orange Flavor – Turbo Black Vitamin brand (all batches)
  • Omega 3 – NB Nutrition brand (all batches)
  • Moringa Oleifera – NB Nutrition brand (all batches)
  • Magnesium Threonate – NB Nutrition brand (all batches)
  • Magnesium DimalaTe – NB Nutrition brand (all batches)
  • Type II Undenatured Collagen – NB Nutrition brand (all batches)
  • Hair, Skin, and Nails – NB Nutrition brand (all batches)
  • Lactoze – Natuforme Produtos Naturais brand (all batches)
  • Ozonized Sunflower Oil – Ozonlife brand (all batches)
  • Premium Maca – Nutrição Esportiva brand (all batches)
  • Max Vision – Turbo Black Vitamin brand (all batches)
  • Hyaluronic Acid + Type II Collagen – NB Nutrition brand (all batches)
  • Concentrated Peruvian Maca – Max Force brand (all batches)
  • Ora-Pro-Nobis Premium – Vitacorpus brand (all batches)
  • All other products manufactured by Ervas Brasillis (all batches)

The Importance of Legislation: What the Law Says

Anvisa’s decision is grounded in national sanitary legislation, particularly Article 46 of Decree-Law 986/1969. This legal provision clearly establishes the obligation for all establishments responsible for the manufacturing, packaging, or transportation of food (including supplements) to obtain prior licensing from the competent health authority—whether at the state, municipal, or district level. The absence of such licensing, along with non-compliance with hygiene and manufacturing standards, constitutes serious violations that justify the agency’s action.

Consult the Official Resolution

For more information and access to the full determination, Resolution RE No. 3,419, dated September 4, 2025, can be accessed directly in the Diário Oficial da União:

www.in.gov.br

× Fale com a gente.