Safety Alert for ACCORDING TO THE ANNEX List ....

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
    1048
  • Date
    2011-02-24
  • 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
    This security alert can be updated at any time. The company undertakes to keep this Agency informed.
  • Reason
    The company st jude informs that, because of having been a victim of accidents, for the health of the population, the products listed in the annex should not be purchased by clients and health professionals.
  • Action
    Those who become aware of the offer of related products should contact the company, ensuring the confidentiality of the informant. St. Jude Medical Brazil Tel. 11 5080 5400 Fax 11 5080 5439 aiwakura@sjm.com lector@sjmbrasil.com br.sjm.com

Device

  • Model / Serial
  • Manufacturer
    N/A

Manufacturer

N/A
  • Source
    ANVSANVISA