Avis De Sécurité sur Accu-Chek Spirit Combo insulin pump (Pumps with serial numbers in the range 10171897 to 10281629 inclusive)

Selon Health Products Regulatory Authority, ce/cet/cette avis de sécurité concerne un dispositif en/au/aux/à Ireland qui a été fabriqué par Roche Diagnostics Ltd..

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
  • Numéro de l'événement
    SN2014(13)
  • Date
    2014-03-24
  • Pays de l'événement
  • Source de l'événement
    HPRA
  • URL de la source de l'événement
  • Notes / Alertes
    "Irish data is current through April 2019. All of the data comes from the Health Products Regulatory Authority (Ireland), 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 Ireland."
  • Notes supplémentaires dans les données
  • Cause
    There is an increased risk that, due to a component change, vibration alarm defects may cause an ‘e-7’ alert message. this fault will be detected at pump start up, when it will display an ‘e-7’ error message and give an audible signal, but will fail to start. the other pump alarms – visual and audible - are not affected by this issue. pumps with serial numbers in the range 10171897 to 10281629 (inclusive) are potentially affected. these pumps were distributed to the irish market between late 2010 and early 2012 and to date, no ‘e-7’ issues related to vibration alarm defects have been reported from ireland.
  • Action
    1. Identify affected pumps.  2. If a delay to insulin therapy could compromise patient safety, consider using an alternative device.  3. When using these pumps:  • Ensure that users are aware of the problem  • Ensure that users have a syringe or insulin pen available in case the pump stops  • If the pump displays an ‘E-7’ error, contact Roche for a replacement device  4. Ensure that appropriate personnel are made aware of this notice. Please also pass this notice on to any end user or organisation where the potentially affected insulin pumps have been transferred

Device

  • Modèle / numéro de série
  • Description du dispositif
    Accu-Chek Spirit Combo insulin pump (Pumps with serial numbers in the range 10171897 to 10281629 inclusive)
  • Manufacturer

Manufacturer