Alerta De Seguridad para Product name: Acrous ultra fast sterilizer //. Technical Name: Sterilizer //. ANVISA registration number: 80511600003 //. Risk class: II - Medium Risk //. Model affected: UR3 //. Serial Numbers Affected: ALL - See Distribution Map

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por ACROUS EQUIPAMENTOS ODONTOLÓGICOS LTDA..

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • ID del evento
    2413
  • Fecha
    2017-11-29
  • País del evento
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
  • Notas / Alertas
    Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.
  • Notas adicionales en la data
    Equipment may only be used for procedures of low risk of transmission of cross-infection through assistance procedures (eg, Orthodontic Intervention Devices or non-critical material). / / Additional information: - Date of identification of the problem by the company: 11/2016 - Notification date for Anvisa: 08/30/2017 The company holding the record of the affected product is responsible for contacting its clients in a timely manner in order to guarantee the effectiveness of the ongoing Field Action. It stands out the joint responsibility of the distribution chain and use of health products in maintaining its quality, safety and efficacy, as well as the effectiveness of the Field Action, expressed by RDC 23/2012: "(...) Art 2 ° A holder of registration of health product is the holder of the registration / registration of health product with Anvisa. Single paragraph. The registration holder, as well as other agents involved from the production to the use of the product, or discarding it when applicable, are jointly and severally responsible for maintaining the quality, safety and efficacy of the health products to the final consumer. Art. 12 Distributors of health products shall forward to the registration holder, in a timely manner, the distribution map and other information requested for the notification and execution of field actions. (...) "
  • Causa
    The equipment does not meet the requirements of a sterilizing equipment for critical materials used in healthcare.
  • Acción
    Field Action Code 170818-01 triggered under the responsibility of the company ACROUS EQUIPAMENTOS ODONTOLÓGICOS LTDA. Company announces Security Alert.

Manufacturer