Alerte De Sécurité sur AVEA PULMONARY FAN - registration 80071310004 - Models no. 17310, 17311, 17312, 17610, 17611, 17612 of all the manufactured units from 01/03/2009 to 06/30/2011.

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par ALLIANCE S/A.

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • ID de l'événement
    1124
  • Date
    2012-04-02
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
    Since the second semester of 2011, from its headquarters in São Paulo / SP, from changes in work orders, changes were observed in some modules of DW (Module responsible for pneumatic controls of the Pulmonary Ventilator) above that considered normal. Since it is a highly complex piece, the company decided to alert its partner (manufacturer) in the USA on these technical issues in order to evaluate the performance of these modules, as it is responsible for the Design Controls of the equipment. From this information, the manufacturer has initiated a series of studies and tests in order to find out the causes of the defects presented by the modules. At the beginning of the year 2012, the manufacturer company realized that the defect could be solved from the change of the TCA plate (Module Command Board). Also, according to the manufacturer, the sequence of alarms presented by the equipment when faulty, is as follows: 1) High Peak Pressure; 2) Safety Valve (Release of Safety Valve); 3) Circuit occlusion; 4) Low PEEP; 5) Low Exhalation Volume. These alarms refer to the equipment sending a high peak pressure to the patient in their ventilatory modes. In this way, the equipment activates the mechanism of releasing the safety valves, releasing the pressure, in order to avoid any possible possibility of harm to the patient. There are no notification records in the NOTIVISA system. Anvisa is following this action.
  • Cause
    Defect on your pneumatic control unit control board.
  • Action
    According to the company's Action Plan, the equipment plates will be changed gradually. In the first stage, the plates will be made by the North American manufacturer. Concurrently, customers will be informed and schedule the exchanges. http://en.wikipedia.org/w/index.php/

Manufacturer

  • Source
    ANVSANVISA