Avis De Sécurité sur Puritan Bennett 800 Series Ventilator System

Selon ALIMS (Agencija za lekove i medicinska sredstva), ce/cet/cette avis de sécurité concerne un dispositif en/au/aux/à Serbia qui a été fabriqué par Covidien LP.

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
    2014-03-02
  • Date de publication de l'événement
    2014-02-28
  • Pays de l'événement
  • Source de l'événement
    ALIMSA
  • URL de la source de l'événement
  • Notes / Alertes
    Serbian data is current through February 2018. All of the data comes from ALIMS (Agencija za lekove i medicinska sredstva), 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 Serbia.
  • Notes supplémentaires dans les données
  • Cause
    Puritan bennett 840 fan users have been provided with conflicting information in the marking supplement (cat. no. 066009a 09/02) that the oxygen sensor should be replaced every two years. the correct useful life is one year from the date of manufacture, as stated in the puritan bennett 840 fan operator's manual. sensor, cat. no. 4-072214-00 sensor kit, pn g-062009-00, should not be used after the expiration date indicated on the oxygen sensor package. the puritan bennett 700 series owner's manual and service instructions also state that the oxygen sensor should be replaced every two years. sensor, cat. no. g-062010-00 i sensor kit, pn g-062009-00, should not be used after the expiration date marked on the oxygen sensor package.

Device

  • Modèle / numéro de série
    cat.num. 066009A, 4-072214-00, G-062010-00, G-062009-00
  • Manufacturer

Manufacturer

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    ALIMSA