Alerta De Seguridad para heartstart xl defibrillator/ monitor battery m3516a

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Philips Healthcare.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2012-10-03
  • Fecha de publicación del evento
    2012-10-03
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: philips heartstart xl defibrillator/ monitor battery m3516a the medicines and healthcare products regulatory agency (mhra), united kingdom and the health canada posted a medical device safety alert concerning heartstart xl defibrillator/monitor battery m3516a, manufactured by philips healthcare. the affected products were labeled with “made in taiwan” and has “r-2011-12” as date of manufacture code. according to philips, the affected battery may not trigger a low battery alarm on the heartstart xl defibrillator/monitor (m4735a). in this case, if the heartstart xl is used on a patient when ac power is not in use, with a battery that may fail, the device may shut down unexpectedly without providing the user with a low battery warning message or audible tone. there is a potential for patient harm if the xl shuts down or becomes inoperable when in clinical use for providing therapy. therefore, philips recommends the following actions: operate the xl with ac power instead of battery power alone. if it is needed to operate the xl on battery power alone, ensure the battery is from a different date of manufacture (it must not have the r-2011-12 date of manufacture code). if unable to operate with ac power alone or locate a battery with a different date of manufacture than that identified above, use an alternative source for treatment or therapy (i.E., backup defibrillator/monitor). according to the local supplier, the affected products have been distributed in hong kong. for details, please refer to the mhra and health canada websites as below: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con185586 http://www.Hc-sc.Gc.Ca/dhp-mps/compli-conform/recall-retrait/_list/rec-ret_md-im_date_oct-dec_2012-eng.Php if you are in possession of the products, please contact your supplier for information and necessary actions. posted on 3 october 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Philips HeartStart XL Defibrillator/ Monitor Battery M3516A
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DH