Alerte De Sécurité sur HOMECHOICE FOR PERITONEAL DIALYSIS. ANVISA Registration No. 10068390123.

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 BAXTER HOSPITALAR LTDA.; Baxter Healthcare SA.

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
    1322
  • Date
    2013-11-04
  • 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
    According to the company, corrective action was initiated due to recent complaints of excess drainage involving patients with hepatic and renal failure using HomeChoice. The patient had ascites (abnormal fluid accumulation in the peritoneal cavity) and according to the report, there was an initial drainage of 6 liters. For the incident, the risk of using HomeChoice (version 10.4) was studied in patients with ascites, as they may present with increased volume of fluid in their peritoneal cavity. The HomeChoice is designed to empty the peritoneal cavity during Initial Drainage, the software with previous versions allowed the operator to stop the active Initial drainage and to avoid it. Software with a current version (version 10.4) allows the operator to stop active initial drainage, but does not allow the operator to avoid it, as it has removed the option of avoiding "active initial drainage" to decrease the unwanted increase in Intraperitoneal volume ( IIPV). Physicians who use the HomeChoice machine to treat patients diagnosed with End Stage Renal Disease who have Ascites should be aware that during treatment the device will attempt to drain the patient for emptying at the start of therapy (Initial Drainage). Patients diagnosed with ascites comorbidity who are drained for emptying may be at high risk of hypotension and compromised hemodynamic status. See detailed information at: http://portal.anvisa.gov.br/wps/wcm/connect/a6d3c40041bb18f49334d79d63c1a945/Carta_ao_cliente.pdf?MOD=AJPERES
  • Cause
    Possibility of excessive drainage involving patients with ascites (abnormal accumulation of fluid in the peritoneal cavity) with use of homechoice.
  • Action
    Complementation of user instructions and safety alert to equipment users.

Manufacturer