Safety Alert for ALL PRODUCTS MANUFACTURED BY THE ANGIPLAST PRIVATE LIMITED COMPANY OF INDIA.

According to Agência Nacional de Vigilância Sanitária (ANVISA), this safety alert involved a device in Brazil that was produced by N/A.

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
    1156
  • Date
    2012-07-26
  • Event Country
  • Event Source
    ANVISA
  • Event Source URL
  • 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
    SEE RESOLUTION - RE Nº 3.172, OF JULY 25, 2012, IN ANNEX.
  • Reason
    Anvisa, by means of resolution - re nº. 3,172, of july 25, 2012, in article 1, determines, as a measure of sanitary interest, the suspension, throughout the national territory, of the importation, distribution, commercialization and use of all products, manufactured by the company, until the company proves compliance with good manufacturing practices.
  • Action
    Suspension throughout the national territory of the importation, distribution, marketing and use of all products manufactured by that company.

Manufacturer

N/A
  • Source
    ANVSANVISA