Events

Retiro De Equipo (Recall) de Acryflex SC60B-0UV

Según L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en France que fue producido por Medical Developmental Research.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • Fecha
    2000-04-10
  • País del evento
    France
  • Fuente del evento
    ANSM
  • URL de la fuente del evento
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/lentilles-intra-oculaires-acryflex-sc60b-0uv-societe-medical-developmental-research
  • Notas / Alertas
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 recall data from the U.S. and France.
  • Notas adicionales en la data
  • Acción
    The director general. Vu. Book VIII of the Public Health Code, and in particular Articles L.793-1 and L.793-5-I. Vu. the three reports of materiovigilance received between 26 September 1999 and 7 February 2000. Seen. the expert report of 8 February 2000. Seen. Mail No. 20000822 dated March 1, 2000, sent to the manufacturer for comments. Considering. that the reports of materiovigilance report four opacifications of Acryflex SC60B-0UV intraocular lenses manufactured and put on the market by the company Medical Developmental Research from December 3, 1997 to March 17, 1999, occurred within 12 to 24 months after their implantation. Considering. to date, the origin of these opacifications, which have led to a decrease in the visual acuity of the patients, could not be determined. Considering. that these opacifications required the explantation of a lens, and that this operation puts patients at risk. Considering. whereas it is therefore appropriate, pending the determination of the causes of the opacifications and in the interest of public health, to suspend the implantation of these lenses. DECIDE. ARTICLE 1. : The distribution, importation and use of Acryflex SC60B-0UV intraocular lenses manufactured by Medical Developmental Research - 2451 Enterprise Road - Clearwater - Florida 33763 - USA, is suspended for a period of 6 months, starting at the date of publication of this Decision. ARTICLE The Director of Medical Device Evaluation and the Director of Inspection and Facilities are responsible, each for his own part, for the implementation of this decision, which will be published in the Official Journal. of the French Republic. Dated at Saint-Denis on April 10, 2000.

Device

Acryflex SC60B-0UV

Manufacturer

Medical Developmental Research
  • Source
    LAANSM