Events

Avis De Sécurité sur Carestation 600

Selon Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), ce/cet/cette avis de sécurité concerne un dispositif en/au/aux/à Slovenia qui a été fabriqué par GE Healthcare.

Qu'est-ce que c'est?

Les avis de sécurité sont des communications que les fabricants de dispositifs médicaux ou leurs représentants font parvenir en particulier aux travailleurs du secteur médical, mais aussi aux utilisateurs de ces dispositifs. Les avis de sécurité concernent les actions entreprises quant aux dispositifs présents sur le marché et peuvent inclure des rappels et des alertes.

En savoir plus sur les données ici
  • Type d'événement
    Field Safety Notice
  • Date
    2016-02-10
  • Pays de l'événement
    Slovenia
  • Source de l'événement
    AMPMDRS
  • Notes / Alertes
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 recall data from the U.S. and Slovenia.
  • Notes supplémentaires dans les données
  • Cause
    The bvt switch may be difficult to move between the operating modes of the mechanical ventilation and the hand bag or it remains in the position and the patient can not be overcome by an anesthetic system. this problem can lead to loss of patient overflow and leads to hypoxia. so far, there have been no reports of injuries or complaints resulting from this problem. if the above problem occurs and no mechanical or manual ventilation mode can be used, a backup method is required for the patient's breathing. if problems with patient overflow occur, use a self-inflating bag immediately. before using the instructions, both in the user manual of the device and in the system's unsupervised system, include instructions on how to check whether the spare spraying, regardless of an anesthetic device, is available and working.

Device

Carestation 600
  • Modèle / numéro de série
    Carestation 620 A1 (GTIN: 00840682103985): SM615020004WA to SM616010008WA; Carestation 650 A1 (GTIN: 00840682103947): SM715020005WA to SM716010008WA; Carestation 650c A1 (GTIN: 00840682103954): SM815020001WA to SM815500001WA.
  • Manufacturer
    GE Healthcare

Manufacturer

GE Healthcare