Alerta De Seguridad para Top Quality - Latex Gloves for Non-Surgical Procedure, with Powder, Registration 80495510001, Extra-small (PP) sizes; Mean (M); Large (G). Lots: Annex I

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por Medix Brasil Produtos Hospitalares e Odontológicos Ltda.; Hartalega SDN..

¿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
    1658
  • Fecha
    2015-07-16
  • 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 semi-annual maintenance tests indicated that the sample analyzed did not meet the "elongation of original rupture" requirement of the INMETRO Ordinance nº332, of June 26, 2012. The health services that have the product in stock must segregate the samples so that the holder of the registration proceed with the collection.//// UPDATE ON 03/15/2015: The OCP informed Anvisa that on February 17, 2012, the suspension of the authorization for the use of the Conformity Identification Seal (Ref 00267- 2) .//// UPDATE 03/22/2016: Field Action completed on 1/8/2016, with collection and destruction of the products.
  • Causa
    Suspension of the authorization for the use of the product identification mark (ocp) compliance identification seal caused by the failure to perform the semi-annual maintenance tests in the attribute "original elongation of rupture", according to reports ela / l-264.770 / 15 ( proof) and ela / l-262.651 / 15 (counter-proof).
  • Acción
    Company is performing Field Action for the product. All lots listed in Annex I shall be collected from the market. More information in the Letter to the Client - Annex II.