Alerta De Seguridad para 3M Scotchcast Wet or Dry Cast Padding

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por 3M.

¿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
    2013-08-07
  • Fecha de publicación del evento
    2013-08-07
  • 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: 3m scotchcast wet or dry cast padding medical device manufacturer, 3m, has issued a medical device safety alert concerning certain lots of scotchcast wet or dry cast padding. the affected catalogue numbers and lot numbers are provided in the following table:- catalogue numbers lot numbers wdp2 792920, 793090, 793640 & 796078 wdp3 792921, 793098, 793638, 796077 & 798487 wdp4 792922, 793116, 793637, 796079, & 798488 wdp6 792923, 793636, 798489, 799235 & 799236 the manufacturer is conducting a voluntary product recall of selected lots of 3m scotchcast wet or dry cast padding following a determination that the cast padding material does not consistently repel water. lack of repellency may result in prolonged cast dry times after exposure to wet conditions. the manufacturer become aware of this issue through health care provider feedback and confirmed it by internal testing. there is a potential of skin maceration under a cast exhibiting inconsistent repellency characteristics. there have been no reports of patient injury associated this material to date. the manufacturer is advising all affected users that currently at the end user setting the captioned cast padding may be used under dry conditions only until replacement product is available. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 07 august 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: 3M Scotchcast Wet or Dry Cast Padding
  • Manufacturer
    3M

Manufacturer

3M