Alerte De Sécurité sur Top Quality - Latex Gloves for Non-Surgical Procedure, with Powder, Registration 80495510001, Extra-small (PP) sizes; Mean (M); Large (G). Lots: Annex I

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par Medix Brasil Produtos Hospitalares e Odontológicos Ltda.; Hartalega SDN..

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • ID de l'événement
    1658
  • Date
    2015-07-16
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
    The semi-annual maintenance tests indicated that the sample analyzed did not meet the "elongation of original rupture" requirement of the INMETRO Ordinance nº332, of June 26, 2012. The health services that have the product in stock must segregate the samples so that the holder of the registration proceed with the collection.//// UPDATE ON 03/15/2015: The OCP informed Anvisa that on February 17, 2012, the suspension of the authorization for the use of the Conformity Identification Seal (Ref 00267- 2) .//// UPDATE 03/22/2016: Field Action completed on 1/8/2016, with collection and destruction of the products.
  • Cause
    Suspension of the authorization for the use of the product identification mark (ocp) compliance identification seal caused by the failure to perform the semi-annual maintenance tests in the attribute "original elongation of rupture", according to reports ela / l-264.770 / 15 ( proof) and ela / l-262.651 / 15 (counter-proof).
  • Action
    Company is performing Field Action for the product. All lots listed in Annex I shall be collected from the market. More information in the Letter to the Client - Annex II.