Ypê keeps two factories idle pending Anvisa’s decision

Detergente Ypê
Photo: Detergente Ypê - Divulgação

Ypê maintains two production units stopped at the Amparo factory complex, inside São Paulo. One plant produces detergents and the other makes washing liquids and disinfectants. The company’s decision came after Anvisa (Agência Nacional of Vigilância Sanitária) identified problems in operations and determined the suspension of part of the product catalog. Segundo the company, approximately 400 employees work three shifts in the affected units.

Ypê’s executive director of Operações, Eduardo Beira, informed that workers from stopped plants were mobilized to accelerate the adjustments required by the regulatory body. The company has a catalog of 450 products, the majority of which are produced in Amparo.

Identificação of products by batch number

Detergente Ypê

The ending 1 in product batches Ypê indicates that they were produced in the complex at Amparo. The information was confirmed during a visit to the factory, when company representatives received journalists the day after revealing details about the health inspection that led to the action. Affected batches include:

  • Lava-crockery with Enzimas Ativas Ypê, Lava-crockery Ypê Clear Care, Lava-crockery Ypê Toque Suave, Lava-crockery Concentrado Ypê Green and variations
  • Lava-Líquido Tixan Ypê clothes in different versions (Combate Mau Odor, Cuida from Roupas, Antibac, Coco and Baunilha, Green), as well as Lava-clothes Ypê Express, Power Act and Premium
  • Desinfetante Bak Ypê, Desinfetante of Uso Geral Atol, Desinfetante Perfumado Atol and Desinfetante Pinho Ypê

The company even suspended Anvisa’s decision after filing an appeal, but chose to keep production stopped to comply with regulatory requirements more quickly.

Problemas identified in inspection

Anvisa identified equipment with signs of corrosion in the inspected facilities. The report also highlighted the inadequate state of conservation of the tank for handling dishwashing products. Fiscais discovered remnants of stored products that were returned to the filling lines, violating quality protocols.

Entre December 2025 and April 2026, the company recorded results outside the microbiological specification in 80 batches of finished products. Entre the findings were the presence of the bacteria Pseudomonas aeruginosa, a pathogen that can cause microbiological contamination. According to the inspection, these batches were not failed by quality control and remained in storage awaiting “financial definition”.

Risco health and contamination

Microbiological contamination refers to the unwanted presence of pathogenic microorganisms such as bacteria, fungi and viruses that produce toxins and can cause illness or irritation. Segundo to Anvisa, the problems identified compromise good manufacturing practices and represent a health risk.

Sobre the batches contaminated with Pseudomonas aeruginosa, the executive director argued that the batches are stored and protected, ensuring that they did not reach consumers. “What we are trying to show is that consumer safety is something that we aim for, that we care about, and as an organization, we would not put anyone’s health at risk,” stated Beira.

Anvisa ordered the suspension of manufacturing and recall of the listed products. The guidance released by the agency was not to use the suspended products until the publication of their analysis. The relevant non-compliances identified included weaknesses in quality assurance, quality control, cleaning, sanitization, validation and microbiological control systems — aspects directly related to the prevention of microbiological deviations.

Próximas steps in the process

Diretoria Colegiada of Anvisa will analyze the case this Wednesday (13). The analysis will discuss whether to maintain or overturn the suspensive effect obtained by Ypê with its administrative appeal. Após In this instance, the case will go through the traditional Anvisa rite, with analysis of the resource itself by Gerência-General of Recursos.

Conforme explained to Alexandre Nemer Elias, a lawyer specializing in health regulatory law, the case should also unfold in parallel follow-ups at Anvisa. The agency will analyze the recall of products by the manufacturer, a procedure that will be monitored by the state Procon and by Secretaria Nacional of Consumidor (Senacon).

The actions determined by Anvisa are suspended until judgment by Diretoria Colegiada. Quando the regulatory agency defines sanctions for companies, resources can be discussed in three instances: initial analysis by the responsible sector, then by Gerência-General of Recursos and, finally, by Diretoria Colegiada as the last internal instance.

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