Alerta De Seguridad para CE INFUSOR Patient Control Module Watch (PCM), 0.5 mL

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Baxter 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
    2015-09-16
  • Fecha de publicación del evento
    2015-09-16
  • 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: baxter ce infusor patient control module watch (pcm), 0.5 ml the medicines and healthcare products regulatory agency (mhra), united kingdom posted a medical device safety alert concerning ce infusor patient control module watch (pcm), 0.5 ml [product code 2c1079k; lot number 15a056 and 15b047], manufactured by baxter healthcare. the manufacturer is issuing a recall for the above affected lots of the infusor pcm, 0.5ml due to complaints for partially detached back-plates on the underside of the device. a partial detachment of the pcm back-plate may cause an incomplete shut-off of the pcm watch tubing resulting in continuous flow of medication from the pcm to the patient. the manufacturer has identified the root cause of this issue and corrective actions have been implemented. the affected lots were produced prior to implementation of the corrective actions. continuous flow of pain medication to the patient may result in sedation, respiratory depression, or respiratory failure resulting in the need for medical intervention. these conditions could lead to serious injury or death. according to the local supplier, the affected products are not distributed in hong kong. for details, please refer to the mhra website:https://www.Gov.Uk/government/publications/safety-information-from-manufacturers-field-safety-notices/field-safety-notices-7-to-11-september-2015 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 16 september 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Baxter CE INFUSOR Patient Control Module Watch (PCM), 0.5 mL
  • Manufacturer

Manufacturer