Alerte De Sécurité sur STERRAD HYDROGEN PEROXIDE CASSETTE, Model STERRAD 100S - Registration 80145900784 - Lots - See Annex 1 - Distribution List

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 Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda.

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
    1370
  • Date
    2014-03-10
  • 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 company informs that there is no impact on the health of the professional or the sterility of the processed devices. Still, it is very unlikely that this event will impact the use of the STERRAD® 100S sterilization system. ASP has already initiated corrective action to eliminate this defect in the manufactured product. • If the STERRAD® 100S sterilization system can not read the bar code, an error message may be displayed: "Can not accept cassette". • If the STERRAD® 100S sterilization system can read the bar code, the injection needles may align incorrectly or one of the following error messages may appear: "Injection Injection System (ISI)" or "Low Injection Pressure 1". In such situations, please read and follow the operating instructions for removing the STERRAD® 100S cassette. • If your STERRAD® 100S system experiences multiple cycle cancellations, it may be due to the damage of the injection needles, which may require a visit by the company's technical support.
  • Cause
    The company holding the record informs that advanced sterilization products - asp has determined that 76 batches of the sterrad® 100s cassette may contain misaligned bar code and can be rejected by the sterrad® 100s sterilization system.
  • Action
    The company requests that customers evaluate the STERRAD® 100S cassette inventory to determine if they are part of the affected batches list below: • If your entire inventory is part of the affected batches list, ASP recommends that the customer continue to use them until it receives lots unaffected, as the probability of damage to the injection needles is low and there is no risk to the health of the professional or the sterility of the processed devices. Once the unaffected batches have been received, the customer may discontinue use of the batches and return them for replacement purposes. • If you have affected and unaffected batches of batches, the batches used should be discontinued and batches sent to the company for replacement. For more information, see Annex 2 - Customer Letter

Manufacturer