Events

Alerta De Seguridad para REGULATORS 2-MODES OF CONTINUOUS VACUUM OHMEDA MEDICAL -: (1) MODEL 67XX-1225-9XX HOUSEHOLD STANDARD TEMPERATURE, (2) MODEL 67XX-1227-9XX LOW TEMPERATURE DOMESTIC PATTERN, (3) MODEL 67XX-1230- 9XX INTERNATIONAL ANTI-TIME SENTIMENT, (4) MODEL 67XX-1233-9XX INTERNATIONAL ANTI-TIME SENSE LOW, (5) MODEL 67XX-1330-9XX DOMESTIC STANDARD SENSE OF TIME HIGH. WE. SERIES GFHD 004234 À GFHD 053409.

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por SQUIRE-COGSWELL/AEROS INSTRUMENTS; OHMEDA MEDICAL AN INSTRUMENTARIUM CO.

¿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
    77
  • Fecha
    2001-05-11
  • 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
    UNTIL THIS DATE DOES NOT CONSERT PRODUCT REGISTRATION IN BRAZIL
  • Causa
    These regulators have incorrect labels. the correction was initiated by ohmeda with the letter sent on 4 and 10 october 2000.
  • Acción
    VERIFY THAT YOU HAVE RECEIVED A LETTER FROM THE OHMEDA OF OCTOBER 2000. IDENTIFY AND ISOLE ANY OF THESE PRODUCTS THAT ARE IN YOUR INVENTORY. TO ORGANIZE THE RETURN OF THE PRODUCTS AFFECTED TO BE CONTACTED BY ITS REPRESENTATIVE OR EMILY DEMSKE, OHMEDA ON THE PHONE (410) 888-5200. FOR FURTHER INFORMATION, CONTACT SQUIRE-COGSWELL / AEROS INSTRUMENTS ON PHONE (847) 855-0800.

Device

REGULATORS 2-MODES OF CONTINUOUS VACUUM OHMEDA MEDICAL -: (1) MODEL 67XX-1225-9XX HOUSEHOLD STAND...

Manufacturer

SQUIRE-COGSWELL/AEROS INSTRUMENTS; OHMEDA MEDICAL AN INSTRUMENTARIUM CO
  • Source
    ANVSANVISA