Events

Alerta De Seguridad para HYDROSOF INTRA-OCULAR LENS ALCON MODEL SH 30 BC

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por ALCON LABORATÓRIOS DO BRASIL LTDA.

¿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
  • ID del evento
    142
  • Fecha
    2001-10-18
  • País del evento
    Brazil
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • Notas / Alertas
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • Notas adicionales en la data
    THE COMPANY REPORTS THAT IT TAKES CLARIFICATION MEASURES TO ITS CLIENTS IN THE SENSE THAT ALL PATIENTS WHO HAVE BEEN IN THE IMPLEMENTED HYDROSOF IOL ARE EXAMINED IN PERIODIC INTERVALS TO DETERMINE IF THERE IS A DECREASE THAT IS AFFECTING THE QUALITY OF THE VISION. AND THAT THE CASES WILL BE REPORTED TO ALCON. IT WILL BE CONTACTED BY THE CUSTOMER SERVICE WHICH IS SENDING TO YOU A LETTER THE RETURN FORM TO BE COMPLETED AND DELIVERED TO THE CARRIER AGENT THAT ALCON SHALL SEND SOON TO REMOVE / REVOKE YOUR REMAINING STOCK, IN THIS CASE THERE IS NO REMAINING STOCK ... YOU SHOULD FAX THE FORM COMPLETED WITH ZERO, AS INSTRUCTED IN THE SAME, AS WELL AS THE SECOND WAY OF THE LETTER. -------------------------------------------------- ----------------- ALCON COMMUNICATION - JULY 17, 2002 - NOTIFY THAT ALL LEGAL PROCEDURES HAVE BEEN COMPLIED WITH THE PROCESS OF COLLECTION OF THE HYDROSOF SH30BC INTRA-OCULAR LENS, HAVING HELD NO DAY 17.04.2002
  • Causa
    Reports on a possible problem with the sh 30bc model of the hydrosof intra-ocular lens. two clinics in brazil reported an excessive level of capsular fibrosis before approximately 45-60 days after surgery, causing the decentration of lenses in some patients. in some cases this can affect the patient's vision in a negative mode. secondary surgical procedures may be needed to replace or replace the intraocular lens and these may cause other complications.
  • Acción
    STILL TO BE NOT ESTABLISHED IF THE PROBLEM IS RELATED TO THE LENS, THE COMPANY IS REQUESTING SURGERIES TO DISCONTINUE THE HYDROSOF IMPLANT PROCEDURE AND RETURN THE REMOTE STOCK FOR ALCON. IT IS RECOMMENDED THAT ALL PATIENTS WHO HAD THE IMPLANTED HYDROSOF IOL BE EXAMINED AT PERIODIC INTERVALS TO DETERMINE THAT THERE IS A DECREASE THAT IS AFFECTING THE QUALITY OF THE VISION AND THAT THOSE CASES ARE REPORTED TO ALCON. RECOMMENDATIONS FOR RETURN / EXCHANGE ... YOU WILL BE CONTAINED BY THE CUSTOMER SERVICE THAT YOU ARE SENDING TO A LETTER THE RETURN FORM TO BE COMPLETED AND DELIVERED TO THE TRANSPORTATION AGENT THAT ALCON SHALL SUBMIT SOON TO REMOVE / REPLACE YOUR STOCK REMANESCENT, IN THIS CASE THERE IS NO REMAINING STOCK ... YOU SHOULD FAX THE FORM COMPLETED WITH ZERO, AS INSTRUCTED IN THE SAME, AS WELL AS THE SECOND WAY OF THE LETTER. REPORT THROUGH THE PHONE 0800-7077993 OR PICK YOUR DAMAGES.

Device

HYDROSOF INTRA-OCULAR LENS ALCON MODEL SH 30 BC

Manufacturer

ALCON LABORATÓRIOS DO BRASIL LTDA
  • Source
    ANVSANVISA