Alerte Ou Avis De Sécurité sur Dynamis and Gerialit with Dewert electrical control systems

Selon Medicines and Healthcare products Regulatory Agency, ce/cet/cette alerte ou avis de sécurité concerne un dispositif en/au/aux/à United Kingdom qui a été fabriqué par Hill-Rom.

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
    Safety alert / Field Safety Notice
  • ID de l'événement
    MDA/2013/031
  • Numéro de l'événement
    CON272240
  • Date
    2013-05-10
  • Date de publication de l'événement
    2013-05-10
  • Pays de l'événement
  • Source de l'événement
    MHRA
  • URL de la source de l'événement
  • Notes / Alertes
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notes supplémentaires dans les données
  • Cause
    Risk of serious injury to patients, staff and visitors. unintentional movement, including sudden collapse to its lowest position, can occur when the bed is connected to the mains supply. a field safety notice (fsn) was published on 01 march 2012.  however, the manufacturer has since advised that these beds should be fixed to their lowest position and the control system deactivated to remove the risk of injury.
  • Action
    Identify affected beds. Consider removing affected beds from use if alternatives are available. If an alternative is not available: consider whether continuing to use the beds at their fixed, lowest position is acceptable if acceptable, fix the beds to their lowest position and contact the manufacturer for instructions on how to deactivate the Dewert control system. Confirm with the manufacturer your actions when completed.

Device

  • Modèle / numéro de série
  • Description du dispositif
    Hospital beds: Dynamis and Gerialit with Dewert electrical control systems. Specific models numbers manufactured from October 1995 to June 2001 inclusive. Dynamis and Gérialit beds were manufactured with electrical control systems supplied by either Dewert or SKF. This notification applies only to Dewert systems, which are easily recognizable by the design of the lockout unit, as shown in the manufacturer’s Field Safety Notice, MOD 466. Affected model numbers: LI146B1—LI146BI, LI146D1—LI146DI, LI147B1—LI147D1, LI150A0—LI150B0, LI163B1—LI163C1, PRS0128, PRS0199, PRS0201, PRS2001.
  • Manufacturer

Manufacturer