Events

Rappel de Device Recall CUSA NXT Ultra Surgical Aspirator System

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Integra LifeSciences Corp..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    56463
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2637-2010
  • Date de mise en oeuvre de l'événement
    2010-07-29
  • Date de publication de l'événement
    2010-09-30
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2012-05-15
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=93733
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    Instrument, ultrasonic surgical - Product Code LFL
  • Cause
    A ground fault malfunction at the rectifier retaining screw may cause the aspiration pump in the cusa nxt service module to run at maximum speed, and continue to run until the entire system is turned off. this may result in excess aspiration that requires medical intervention.
  • Action
    Integra issued Urgent: Product Recall Notification letters dated July 29, 2010 to all customers on July 29, 2010 identifying the affected products, issue prompting the recall, and actions to be taken by the customer. Letters were also forwarded to all Integra Account Reps. Customers were advised to discontinue use of and quarantine the affected service modules. The Surgical Aspirator may be operated without the Service Module, utilizing the hospitals wall aspiration. Company representatives will contact customers to arrange product return and repair of the affected service modules. Customers are to complete and return an enclosed Recall Acknowledgement and Return Form. The firm can be contacted at 609 936-2485.

Device

Device Recall CUSA NXT Ultra Surgical Aspirator System
  • Modèle / numéro de série
    Serial numbers: NXT1001-1079, NLB0901901IE, NBL0902101IE, NBL0902501IE, NBA1000501IE, NBC1001501IE, NBC1002001IE, NBC1002301IE, NBC1002901IE, NBE1001301IE, NCE1001901IE, NBF1000701IE, NBD1000101IE.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    Unclassified
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution: USA , including the states of AZ, CA, CO, FL, GA, IA, KY, MN, MO, NV, NY, OH, OR, RI, TX, VA, WI, and the countries of Germany, Hungary, Indonesia, Italy, Netherlands, and Switzerland.
  • Description du dispositif
    Integra CUSA Ultrasonics NXT Ultra Surgical Aspirator System || CUSANXT1:Latex Free, Rx only: || Integra LifeSciences (Ireland) Limited, || County Offaly, Ireland; || Distributed by Integra Life Sciences Corporation || 311 Enterprise Drive || Plainsboro, NJ 08536.
  • Manufacturer
    Integra LifeSciences Corp.

Manufacturer

Integra LifeSciences Corp.