Alerte De Sécurité sur BVM (Bag-Valve-Mask) Manual Resuscitation Systems

Selon Department of Health, ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Hong Kong qui a été fabriqué par Intersurgical Ltd.

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
  • Date
    2018-01-09
  • Date de publication de l'événement
    2018-01-09
  • Pays de l'événement
  • Source de l'événement
    DH
  • URL de la source de l'événement
  • Notes / Alertes
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 Hong Kong.
  • Notes supplémentaires dans les données
    Medical Device Safety Alert
  • Cause
    Medical device safety alert: intersurgical ltd bvm (bag-valve-mask) manual resuscitation systems the medicines and healthcare products regulatory agency (mhra) of the united kingdom posted a field safety notice concerning bvm (bag-valve-mask) manual resuscitation systems, manufactured by intersurgical ltd. the affected devices are identified as the following:- reference numbers (lot numbers): 7150000 (363791, 370252, 370751, 371638, 372887, 372894, 375508) 7151000 (364909, 370253, 371091, 371639, 372886, 372890, 375711) 7152000 (363792, 364270, 364923, 365216, 370266, 370752, 371640, 371656, 372888, 372889, 372893, 373638, 373639, 375411) 7152005 (31753284, 31756956, 31757575) 7152006 (31660106, 31753127, 31756716, 31757576, 31758289) 7152007 (371092) 7152012 (31753733, 31756957) 7153000 (363793, 370738, 371907, 372892, 375509) 7153008 (31753734) 7154000 (370753, 372367) a manufacturing fault has been identified with the intersurgical bvm manual resuscitation system, which could result in the directional valves positioned on the ‘back plate’ of the self-inflating bag being orientated incorrectly. the incorrect orientation of the directional valves could result in the bvm manual system becoming over pressurised, which could result in patient barotrauma. according to the manufacturer, bvm manual resuscitation systems with alternative directional valves configuration positioned on the ‘back plate’ are not affected by this fsn and are safe to use. affected users are instructed to quarantine and stop the use of all affected devices. if no suitable replacement is available, users should check the orientation of the valves on the back plate of the self-inflating bag and ensure they are orientated correctly. for details, please refer to the mhra website: https://www.Gov.Uk/drug-device-alerts/field-safety-notice-2-to-5-january-2018 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 09 january 2018.

Device

  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Intersurgical Ltd BVM (Bag-Valve-Mask) Manual Resuscitation Systems
  • Manufacturer

Manufacturer