Events

Rappel de Covidien Curity Eye Pad, Curity Eye Pad Oval, Curity Sodium Chloride Dressing Covidien Curity Eye Pad

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Covidien Pty Ltd.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    RC-2017-RN-00354-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2017-03-17
  • Pays de l'événement
    Australia
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2017-RN-00354-1
  • Notes / Alertes
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • Notes supplémentaires dans les données
  • Cause
    There is a potential for the sterile packaging of the covidien curity eye pad, curity eye pad oval and curity sodium chloride dressing to be compromised. hence, the use of products with this issue may result in an increased risk of infection. to date, there have been no reports of infection associated with this issue.
  • Action
    Medtronic is advising customers to quarantine and discontinue the use of affected stock. Customers are also requested to label the stock with the provided ZRE # (number) prior to their return to Medtronic whereby customers will receive credit to the value of the returned stock.

Device

Covidien Curity Eye Pad, Curity Eye Pad Oval, Curity Sodium Chloride Dressing Covidien Curity Eye...
  • Modèle / numéro de série
    Covidien Curity Eye Pad, Curity Eye Pad Oval, Curity Sodium Chloride Dressing Covidien Curity Eye Pad Item Code: 03201Lot Numbers beginning with 12, 13, 14, 15 and16Covidien Curity Eye Pad OvalItem Code: 2841Lot Numbers beginning with 12, 13, 14, 15 and16Covidien Curity Sodium Chloride Dressing Item Code: 3339Lot Number beginning with 14, 15, 16 (Excluding lots: 16J098062, 16J098162, 16J098262)ARTG Numbers: 186368, 186373
  • Manufacturer
    Covidien Pty Ltd

Manufacturer

Covidien Pty Ltd
  • Société-mère du fabricant (2017)
    Medtronic plc
  • 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
    DHTGA