Events

Alerte De Sécurité sur SONY LMD-1951MD Monitors used with SpyGlass

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

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
    2015-03-12
  • Date de publication de l'événement
    2015-03-12
  • 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_20150312a.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: sony lmd-1951md monitors used with spyglass medical device manufacturer, boston scientific, on behalf of sony electronics inc., has issued a field safety notice concerning specific sony lmd-1951md monitors (material numbers: m00546120, m0054612s0, m0054612z0) used with spyglass. according to the manufacturer, the monitor may either not turn on, or may lose image during use in some situations. the issue is the result of a potential disconnection of the internal power supply caused by a failure of a power board integrated circuit. the failure mode does not occur when an ac adapter is used with the monitor. as a precautionary measure, the manufacturer asks all users to take the following actions. if users possess an ac adapter for each of the affected monitors, use only the ac adaptor when the monitors are in use. users who do not possess an ac adapter for each of the affected monitors should stop using the monitor and take the monitor out of service until the permanent corrective action described below is implemented. as a permanent corrective action, the manufacturer will replace the power board of all affected units with a redesigned power board that does not exhibit this failure mode. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 12 march 2015.

Device

SONY LMD-1951MD Monitors used with SpyGlass
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: SONY LMD-1951MD Monitors used with SpyGlass
  • Manufacturer
    Boston Scientific

Manufacturer

Boston Scientific
  • Société-mère du fabricant (2017)
    Boston Scientific
  • Commentaire du fabricant
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    DH