Alerte De Sécurité sur sterile gauze pad - 9 threads / cm2 - 7,5cmx7,5cm - carton with 240 envelopes with 10 units - product code 217612 Lot: 6003268/39 - quantity 60 cartons ////. . sterile gauze pad - 11 threads / cm2 - 7,5cmx7,5cm - box with 240 envelopes with 10 units - product code 194586 Lot: 6003269/39 - quantity 120 boxes; . sterile gauze pad - 11 threads / cm2 - 7,5cmx7,5cm - box with 50 envelopes with 10 units - product code 197075 Batch: 6003269/39 - quantity 120 boxes; ///. . sterile gauze pad - 13 threads / cm2 - 7,5cmx7,5cm - carton with 240 envelopes with 10 units - product code 194579 Batch: 6003269/40 - quantity 30 cartons ///. . sterile gauze pad - 11 threads / cm2 - 100 cm x 91 cm - box with 120 units - product code 232851 Batch: 6003265/39 - quantity 29 cartons ///. . Sterile Vaginal speculum - small size - box with 100 units - product code 230468 - Lot: 6003240/36 - quantity: 10 boxes;

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 CREMER S/A.

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
    753
  • Date
    2003-10-24
  • 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
    considering the provisions in Article 6 of Law no. 9,782, of January 26, 1999; considering the provisions of Article 6, Item I, and Article 12, paragraph 3, Section III, of Law no. 8,078, of September 11, 1990; considering the Theft Communication of Products for Health, of the company CREMER S / A; considering the Boletim de Occurência nº 178/2003, issued by the 6th Precinct of Investigation on Narcotics and General Investigations Service of Jacupiranga / SP DEINTER 6
  • Cause
    Complete batches of stolen health products.
  • Action
    To determine, as a measure of health interest, the seizure, in the whole national territory, of the related products, since they are full batches of stolen health products.

Manufacturer

  • Source
    ANVSANVISA