Alerta De Seguridad para avaira toric and biocomfort xo toric contact lenses

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

¿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
    2011-08-22
  • 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
    Press release
  • Causa
    Recall of avaira toric and biocomfort xo toric contact lenses subsequent to department of health’s (dh’s) advice on suspension of use of avaira toric contact lenses over the weekend, the dh today (august 22) endorsed the recall of the avaira toric contact lenses and another product biocomfort xo toric contact lenses because further information from the distributor, coopervision hong kong, revealed that the product marketed as biocomfort xo toric brand, was the same product as avaira toric contact lenses in hong kong. a dh spokesman said upon further investigation, coopervision revealed that both the biocomfort xo toric and avaira toric were manufactured by the same manufacturer and the same production line. the biocomfort xo toric had been directly marketed only to the members of the hong kong association of private practice optometrists (appo) at their shops. dh advised over the weekend that consumers should suspend use of avaira toric contact lenses.  the advice followed the recall of avaira toric in the united states, australia, canada, germany, italy and spain after investigating into complaints of discomfort and/or blurred vision from consumers, which were likely to be due to transient swelling of the surface layer of the corneas brought about by a small amount of residues on the lens. consumers should also suspend the use of biocomfort xo toric because of the same defect. the spokesman further explained that in view of possible consumer safety concern, a total recall of the two products is a prudent measure. coopervision admitted that as revealed by the information at hand, the two products were the affected products identified so far.  dh will continue the investigation. dh had already alerted the hospital authority, private hospitals, relevant healthcare institutions and medical associations about the matter. coopervision hongkong has issued a letter to related eye care practitioners regarding the recall. the company has also set up a hotline at 3718 0602 to answer enquiries between 9 am and 5 pm from monday to friday. the spokesman said dh has so far not received any adverse reports arising from use of the products. "members of the public should consult their healthcare providers when in doubt and in particular, if they feel unwell after using the products. dh will continue the investigation and closely monitor the recall.” ends/.

Device

  • Modelo / Serial
  • Clasificación del producto
  • Descripción del producto
    Press release: Recall of Avaira Toric and BioComfort XO Toric contact lenses
  • Manufacturer

Manufacturer