Alerte De Sécurité sur Infusomat Compact - Infusomat Compact Infusion Pump / Infusion Pump Technical Name: Infusion Pump ANVISA Registration Number: 10008530367 Hazard Class: III Model Affected: Infusomat compact

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 Laboratórios B. Braun S.A.; Laboratórios B. Braun S.A..

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
  • Date
  • Pays de l'événement
  • Source de l'événement
  • 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
    To take measures to ensure the safe use of the units of equipment belonging to the serial numbers involved in this field action, proceeding, in case of need of change of flow during therapy, using the "titration" function, as described in the User Manual, Rev. 10 page 30. Then, fill in the data contained in the field action notification letter and notify B. Braun Laboratories that software 4.00 will be replaced by software 3.05.
  • Cause
    There were three situations of undesired operation in infusomat compact devices with software version 4.00 (sw 4.00), as described below: 1. when it is desired to change the flow through the "c" key with the infusion in progress as described in the manual the user, rev.10. p. 30, the number key "8" is inhibited, ie when this key is pressed, the digit 8 is not added to the flow value. however, due to the need to change the flow rate to increase or decrease it, according to medical prescription, during the infusion, the titration function (described in the user manual rev.10 page 30) can be used without any difficulty, taking into account need for infusion therapy. titration is the most recommended and used procedure in hospital practice. 2. when the equipment is switched on and then a drug is selected without programming or starting the infusion, the device does not allow the flow to be programmed without the "c" key being pressed. only the numeric keys 7, 8, 9 and 0 are expected to function without the "c" key being pressed. 3. if the infusion is intentionally interrupted or programmed without the infusion being started / started by the start key, after four minutes the device sounds a continuous alarm (expected only in case the pump is awaiting infusion start) and after a few seconds it starts to emit repetitive beeps.
  • Action
    Field Action Code AC / 05/2016 triggered under the responsibility of the company Laboratorios B. Braun SA Company will make correction in the field.