Alerta De Seguridad para All products produced by the company Meta Bio Industrial Ltda for valid product registrations, these being: 80034760001; 80034760003; 80034760004; 80034760005; 80034760006; 80034760007; 80034760008; 80034760009; 80034760010; 80034760011; 80034760012; 80034760014; 80034760015; 80034760016; 80034760017; 80034760018; 80034760019; 80034760020; 80034760021; 80034760022; 80034760023; 80034760024; 80034760025; 80034760026; 80034760027; 80034760028; 80034760029; 80034760030; 80034760031; 80034760032; 80034760033; 80034760034; 80034760035; 80034760036; 80034760037; 80034760038; 80034760039; 80034760040; 80034760041; 80034760042; 80034760043; 80034760044; 80034760045; 80034760046; 80034760047; 80034760048; 80034760049; 80034760050; 80034760050; 80034760051; 80034760052; 80034760053; 80034760054; 80034760055; 80034760056; 80034760057; 80034760058; 80034760059; 80034760060; 80034769001

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por Meta Bio Industrial 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
    1780
  • Fecha
    2015-12-21
  • 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
    The UI, although not in accordance with the latest version of the registry, provides all necessary information regarding the manufacturer's information, indications of use for each type of product / product line, contraindications, special care, postoperative complications, information to the patient, adverse effects, information to the attending physician, conditions and precautions with transportation, handling, storage and preservation, product traceability, product disposal, safe implant removal, identification of product records and all information necessary to that any person or institution can contact Meta Bio or ANVISA via Notivisa. It is important to note that so far there has been no technical complaint, consultation of clients or any health professional questioning the current instructions for use or the content thereof.
  • Causa
    The instructions for use on the products (all registrations) were not in accordance with the latest versions published and approved in their respective anvisa product registers.
  • Acción
    a) Risk classification: III b) Classification of the field action: Update, correction or compelmentation of the Instructions for Use c) Field action code: IU / 2015 d) recommendations to users and patients: By publishing the Alert Message Meta Bio, we request that our Distributors disregard the Instructions for Use currently packaged with the products and then consider those published electronically on the Meta Bio website. It is not necessary to follow-up the implanted patients, since the Instruction of Use is not for the lay public and contains information necessary for the due contacts of any type of complaint or adverse event.

Manufacturer