Rappel de Philips Gel-E Donut and Squishon 2 (Gel filled Pillow)

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Philips Electronics Australia 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-2014-RN-00773-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2014-07-18
  • Pays de l'événement
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
  • 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
    Philips healthcare has received a number of complaints about visible mould on gel-e donut and squishon 2 gel-filled products. the mould manifests as small black markings on the outer surface of the gel-e donut and squishon pad, which are visible through the transparent outer packaging. the mould detected on the product has been cladosporium and penicillium fungi, which are commonly found moulds. nicu and picu patients are much more sensitive to moulds and there is potential for the mould to be transferred to these environments once the outer pack is opened.
  • Action
    Users are advised to review their entire inventory of Gel-E Donut and Squishon 2 products and inspect each product for signs of visible mold. Mold should be readily seen as black dots or splotches through the transparent outer packaging. Please do not open the packaging to do the inspection. If unsure or if the inspection is inconclusive, please err on the side of caution and designate that product as containing mold. Dispose of any product containing mold per facility’s environmental guidelines and return unaffected product to their inventory. Customers are also referred to the Instructions for Use, in particular: Wipe all Gel product surfaces with an antibacterial agent and cover the Gel product with a disposable cover or soft cloth before patient use. This action has been closed-out on 17/08/2016.

Device

  • Modèle / numéro de série
    Philips Gel-E Donut and Squishon 2 (Gel filled Pillow)Part numbers: 92025-A, 92025-B, 92025-C (Gel-E Donut) and 91033-2 (Squishon 2)ARTG number: 200647
  • Manufacturer

Manufacturer

  • Société-mère du fabricant (2017)
  • Source
    DHTGA