Events

Rappel de Device Recall SpheRx Posted Pedicle Screw 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 NuVasive Inc.

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
    52634
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0367-2013
  • Date de mise en oeuvre de l'événement
    2009-01-05
  • Date de publication de l'événement
    2012-11-19
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2012-11-19
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=83516
  • 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
    Orthosis, spinal pedicle fixation, for degenerative disc disease - Product Code NKB
  • Cause
    The tulip portion of the screw assembly can disengage from the shank after implantation.
  • Action
    Telephone communications to the sales representatives of surgeons actively using the Posted Pedicle Screw System were made on 01/05/2009. The calls were unscripted and requested that all inventory be forwarded to NuVasive's San Diego office for quarantine. Surgeons who were actively using the system were also contacted and notified of the situation. Follow-up communications were sent via mail on 01/19/2009 to all surgeons who participated in the Alpha release. The letter informed the customers of the problems identified. Customers were instructed that the recalling firm does not believe any further action is required and they were instructed to monitor the progress of their patients and notify NuVasive if any issues are detected. Customers with questions or concerns are instructed to contact the firm at (858) 909-1964.

Device

Device Recall SpheRx Posted Pedicle Screw System
  • Modèle / numéro de série
    Batch: JK1949, JK2068, JK2071, JK2078, JK2079, JK2170, JK2206, JK2375, JK2387, JK2398, JK2400
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution-including the states of OR, MO, FL, WI, CA, and NC.
  • Description du dispositif
    Screw Tulip , 5.5mm Rod || Subsequent Codes: KWP, KWQ, MNH, MNI
  • Manufacturer
    NuVasive Inc

Manufacturer

NuVasive Inc
  • Adresse du fabricant
    NuVasive Inc, 7475 Lusk Blvd, San Diego CA 92121-5707
  • Société-mère du fabricant (2017)
    NuVasive, Inc.
  • Source
    USFDA