Events

Alerte De Sécurité sur I-stat 1 Analyzer system - G3+ Cartridge

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

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
    2014-03-21
  • Date de publication de l'événement
    2014-03-21
  • Pays de l'événement
    Hong Kong
  • Source de l'événement
    DH
  • URL de la source de l'événement
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20140321.html
  • 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: abbott i-stat 1 analyzer system - g3+ cartridge health canada has issued a medical device safety alert concerning i-stat 1 analyzer system - g3+ cartridge, manufactured by abbott point of care inc. the affected model number is 03p78-25, and the affected lot number is n13183. the manufacturer has determined that i-stat g3+ cartridges from cartridge lot number n13183 have the potential to exhibit incorrectly elevated partial pressure of carbon dioxide (pco2) and depressed ph results. the pco2 results can be elevated by 10 to 25 mmhg while the ph results can be depressed by 0.10 to 0.15. all other g3+ cartridge lots are unaffected by this issue. for details, please visit the following health canada website: http://www.Healthycanadians.Gc.Ca/recall-alert-rappel-avis/hc-sc/2014/38453r-eng.Php if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 21 march 2014.

Device

I-stat 1 Analyzer system - G3+ Cartridge
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Abbott I-stat 1 Analyzer system - G3+ Cartridge
  • Manufacturer
    Abbott Point of Care Inc

Manufacturer

Abbott Point of Care Inc
  • Société-mère du fabricant (2017)
    Abbott Laboratories
  • Commentaire du fabricant
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    DH