Rappel de DePuy Synthes TI Vectra Plates

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 Synthes, 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
    69178
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2674-2014
  • Date de mise en oeuvre de l'événement
    2014-09-02
  • Date de publication de l'événement
    2014-09-22
  • Statut de l'événement
    Terminated
  • Pays de l'événement
  • Date de fin de l'événement
    2015-09-02
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
  • 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
    Appliance, fixation, spinal intervertebral body - Product Code KWQ
  • Cause
    Depuy synthes is initiating a voluntary medical device recall of certain lots of the ti vectra plates, which is a part of the depuy synthes vectra anterior cervical plate family of systems. the vectra systems are intended for anterior screw fixation to the cervical spine (c2-c7). it was discovered in certain lots, that the clips are potentially missing from the ti vectra plates resulting in the i.
  • Action
    DePuy Synthes sent an Urgent Notice Medical Device Recall letter dated September 2, 2014, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Please take the following actions: If you DO have any of the identified devices, please take the following steps: Call DePuy Synthes at 1-800-479-6329 to obtain a Return Authorization (RA) Number. Complete the Verification Section (page 3 of this letter) by checking the appropriate box indicating affected product has been located. Also, please indicate the number of devices found and note the Return Authorization Number. Please include your name, title, address, telephone number and signature in the spaces provided. Return the Verification Section (page 3 of this letter) with the product to: Credit/Returns, DePuy Synthes, 1101 Synthes Avenue, Monument, CO 80132. Send a copy of the completed Verification Section to DePuy Synthes by: Fax: (610) 430-7083 or Scan/email: Fieldaction@synthes.com If you DO NOT have the identified product, please take the following steps: Complete the attached Verification Section (page 3 of this letter) by checking the appropriate box indicating that no affected product has been located. Please include your name, title, address, telephone number and signature in the spaces provided. This return documentation acknowledges your receipt of medical information. Return the documents to DePuy Synthes by: Fax: (610) 430-7083 or Scan/email: Fieldaction@sythes.com Note: If the Verification Section is answered on behalf of more than one facility and/or individual, please clearly indicate the name and address of the facility and/or individual on page 3 of the notification. If you have any questions, please call 610-719-5450, or contact your DePuy Synthes sales consultant.

Device

  • Modèle / numéro de série
    TI Vectra-One" Plate 2 Level / 34 mm  part 04.613.184  3337672  TI Vectra" Plate 3 Level / 57 mm  part 04.613.257  lot 3693878  TI Vectra" Plate 4 Level / 64 mm  part 04.613.364  lot 8143905
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    US Distribution including the states of IL, SC, VA, TX, MA, NC, LA, CA, AL, CO, NE, OR and KS., and Internationally to Canada.
  • Description du dispositif
    DePuy Synthes TI Vectra Plates: || TI Vectra-One" Plate 2 Level / 34 mm || part 04.613.184 || 3337672 || TI Vectra" Plate 3 Level / 57 mm || part 04.613.257 || lot 3693878 || TI Vectra" Plate 4 Level / 64 mm || part 04.613.364 || lot 8143905
  • Manufacturer

Manufacturer

  • Adresse du fabricant
    Synthes, Inc., 1302 Wrights Ln E, West Chester PA 19380-3417
  • Société-mère du fabricant (2017)
  • Source
    USFDA