Events

Alerte De Sécurité sur Ventlab manual resuscitators

Selon Department of Health, ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Hong Kong qui a été fabriqué par Ventlab Corporation.

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
  • Date
    2012-10-24
  • Date de publication de l'événement
    2012-10-24
  • Pays de l'événement
    Hong Kong
  • Source de l'événement
    DH
  • URL de la source de l'événement
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20121024.html
  • Notes / Alertes
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 Hong Kong.
  • Notes supplémentaires dans les données
    Medical Device Safety Alert
  • Cause
    Medical device safety alert: ventlab manual resuscitators the united states food and drug administration (fda) has posted a firm press release concerning ventlab manual resuscitators distributed between march 2012 and july 2012. ventlab corporation, the device manufacturer, initiated a nationwide recall of 14,602 of its manual resuscitators. the manual resuscitators, as listed below have been found to potentially deliver little to no air/oxygen through the patient valve to the patient, which could result in life threatening health consequences that include hypoxia and hypoventilation. the recall includes the following product models: ventlab airflow adult resuscitator ventlab airflow infant resuscitator ventlab airflow small adult resuscitator ventlab statcheck adult resuscitator ventlab safespot infant resuscitator ventlab premium infant resuscitator ventlab premium small child resuscitator ventlab premium small adult resuscitator ventlab rescuemed infant resuscitator breathtech safespot infant resuscitator provider enterprises safespot infant resuscitator provider enterprises adult resuscitator the manufacturer voluntarily recalled the above listed products after becoming aware of a product incident where the nature of the complaint was that the resuscitators were delivering little or no air through the patient valve to the patient. no injuries have been reported to-date. end users who have these manual resuscitators should stop using them and immediately contact ventlab corporation or your supplier for further instructions on the return of these products. for details, please refer to the following fda website http://www.Fda.Gov/safety/recalls/ucm324561.Htm if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 24 october 2012.

Device

Ventlab manual resuscitators
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Ventlab manual resuscitators
  • Manufacturer
    Ventlab Corporation

Manufacturer

Ventlab Corporation