Events

Rappel de Device Recall Apex Knee 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 OMNIlife science 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
    79268
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1117-2018
  • Date de mise en oeuvre de l'événement
    2017-11-20
  • Statut de l'événement
    Completed
  • Pays de l'événement
    United States
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=161796
  • 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
    Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer - Product Code JWH
  • Cause
    The apex knee system tibial baseplate identified has an improper expiration date marked on the external packaging. the improper expiration date (2202-03) is marked on the external packaging only. the correct lot number (2022-03) is present in the internal packaging and sterile batch documentation.
  • Action
    OMNIlife science, Inc. sent an Urgent Medical Device Advisory Notice dated November 20, 2017. Actions to be taken by the Customer/User "Immediately quarantine lot 26519 for KC-2206L "Return Product Using RMA# XXXX to OMNI. "This advisory notice only includes LOT 26519. It does not affect other lots. You must acknowledge this notice by returning the attached Acknowledgement and Receipt Form and accompanying by FAX to 508-819-3390 or my email to CS@omnils.com. For further questions, please call (508) 824-2444.

Device

Device Recall Apex Knee System
  • Modèle / numéro de série
    Product Code KC-2206L, Lot # 26519
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - US Distribution and to the country Spain.
  • Description du dispositif
    Apex Knee System, Tibial Baseplate Size 6 Left, non-porous - KC-2206L || The Apex Knee System is intended for use as a primary or revision total knee replacement. This knee replacement system is intended for cemented fixation and single use implantation. This prosthesis may be used for the following conditions, as appropriate: Non-inflammatory degenerative joint disease, including osteoarthritis and avascular necrosis; Rheumatoid arthritis; Correction of functional deformity; Revision procedures where other treatments or devices have failed.
  • Manufacturer
    OMNIlife science Inc.

Manufacturer

OMNIlife science Inc.
  • Adresse du fabricant
    OMNIlife science Inc., 480 Paramount Dr, Raynham MA 02767-1085
  • Société-mère du fabricant (2017)
    Omnilife Science Inc
  • Source
    USFDA