Events

Rappel de DuraGuard Dural Repair Patch

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 Synovis Surgical Innovations, 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
    66763
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-0339-2014
  • Date de mise en oeuvre de l'événement
    2013-10-28
  • Date de publication de l'événement
    2013-11-18
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2014-06-03
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=123332
  • 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
    Dura substitute - Product Code GXQ
  • Cause
    Synovis, a subsidiary of baxter international inc., is recalling certain shipments of vascuguard and dura-guard because synovis, a subsidiary of baxter international inc., is recalling certain shipments of vascuguard and dura-guard because the shipping configurations in which the 6 fluid ounce units containing a specific revision of the instructions for use (ifu) shipped in a divided cell shipping.
  • Action
    A customer notification letter dated 10/28/13 was sent to all customers who purchased the Vascu Guard and the Dura Guard. The letter informs the customers of the problem identified and the actions to be taken. Customers with any questions regarding the recall are instructed to contact Customer Service unit at (800) 423-2090. If customers are distributors or if they have have distributed the recalled products to any other health care provider, they are instructed to notify their accounts and provide them with a copy of the recall notification. If customers would like Baxter to perform the recall task for them, then they are instructed to contact Stericycle at 1-866-912-8417.

Device

DuraGuard Dural Repair Patch
  • Modèle / numéro de série
    Lot Numbers:  SPCE113-03C0006 SPCE113-04D0002 SPCE113-04D0047 SPCE113-05E0052 SPCE113-05E0072 SPCE113-07G0077 SPCE113-08H0018 SPCE113-08H0073 SPCE113-03C0008 SPCE113-03C0072 SPCE113-04D0036 SPCE113-04D0092 SPCE113-04D0093 SPCE113-05E0047 SPCE113-05E0048 SPCE113-06F0053 SPCE113-06F0054 SPCE113-07G0008 SPCE113-07G0072 SPCE113-08H0016 SPCE113-FEB0092 SPCE113-JAN0046 SPCE113-JAN0106 SPCE113-03C0004 SPCE113-03C0069 SPCE113-03C0070 SPCE113-03C0071 SPCE113-04D0085 SPCE113-04D0086 SPCE113-05E0073 SPCE113-05E0074 SPCE113-06F0055 SPCE113-06F0057 SPCE113-06F0138 SPCE113-06F0139 SPCE113-07G0074 SPCE113-07G0075 SPCE113-08H0019 SPCE113-JAN0047 SPCE113-JAN0048 SPCE113-JAN0109 SPCE113-JAN0125
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Dura Guard, Dural Repair Patch with Apex Processing. || For use as a dura substitute for the closure of dura mater during neurosurgery. || Product Code: || DG0209SN || DG0209SN || DG0209SN || DG0209SN || DG0209SN || DG0209SN || DG0209SN || DG0209SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0404SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN || DG0608SN
  • Manufacturer
    Synovis Surgical Innovations, Inc.

Manufacturer

Synovis Surgical Innovations, Inc.
  • Adresse du fabricant
    Synovis Surgical Innovations, Inc., 2575 University Ave W, Saint Paul MN 55114-1073
  • Société-mère du fabricant (2017)
    Baxter International
  • Source
    USFDA