Events

Safety Alert for all products manufactured by the company that manufactures medical-dental equipment, MZ INDÚSTRIA E COMÉRCIO LTDA

According to Agência Nacional de Vigilância Sanitária (ANVISA), this safety alert involved a device in Brazil that was produced by MZ INDÚSTRIA E COMÉRCIO LTDA.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Event ID
    751
  • Date
    2003-10-30
  • Event Country
    Brazil
  • Event Source
    ANVISA
  • Event Source URL
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • Notes / Alerts
    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.
  • Extra notes in the data
    considering paragraph 3 of art. 111 of the Internal Regulation approved by Administrative Rule no. 593 of August 25, 2000, republished in the Official Gazette of December 22, 2000; considering the arts. 12 and 25 of Law no. 6,360, September 23, 1976; considering items XXIX, XXXV of art. 10, of Law no. No. 6,437, August 20, 1977; considering items IX, X, XV, XXIV, all of art. 7 of Law No. 9,782, of January 26, 1999; considering CVS communiqué 350/2003 GT Correlatos DITEP, published in the Official Gazette of the State of São Paulo on October 16, 2003, regarding the Notice of Infringement No. 01015 ¿AIP 01059 and TIP 02464, drawn up by the Municipal Health Department of Ribeirão Black, on the 25th day of February 2003
  • Reason
    Do not have registration with anvisa, imposing health risk.
  • Action
    Determine, as a measure of sanitary interest, throughout Brazil, the suspension of the manufacture and sale of all products manufactured by the company that manufactures medical-dental equipment, MZ INDÚSTRIA E COMÉRCIO LTDA, at Rua Santos nº 1121, Vila Elisa , Ribeirão Preto / SP, for not having registered with ANVISA, imposing health risk.

Device

all products manufactured by the company that manufactures medical-dental equipment, MZ INDÚSTRIA...

Manufacturer

MZ INDÚSTRIA E COMÉRCIO LTDA
  • Source
    ANVSANVISA