Events

Rappel de Device Recall LeMaitre Vascular AnastoClip AC Closure 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 LeMaitre Vascular, 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
    74563
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-2283-2016
  • Date de mise en oeuvre de l'événement
    2016-06-22
  • Statut de l'événement
    Open, Classified
  • 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=147905
  • 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
    Clip, implantable - Product Code FZP
  • Cause
    Us marketing brochure for the anastoclip ac closure system states that the anastoclip catalog numbers can be used for dura closure, but the catalog numbers are only intended for cardiovascular use.
  • Action
    The firm, LeMaitre Vascular, Inc., sent an "URGENT: Medical Device Correction" letter dated June 20, 2016 to its distributors and hospitals via Priority mail. The letter describes the product, problem and actions to be taken. The customers were informed of the intended use of the devices and the correct catalog numbers to order for the dura application. The customers were instructed to return unused devices for an exchange or refund; destroy any Anastoclip related marketing materials that you have received from Lemaitre between October 25- 2015 and June 15, 2016, and complete and return the reply form for reconciliation of this recall via fax at 781-221-2223, email: CSUS@LEMAITRE.COM or by mail. LeMaitre Vascular, Inc. will replace any affected device with a new device labeled for dura closure or issue a credit per request. Questions concerning this safety notice, please contact me at 781-221-2266 ext. 183.

Device

Device Recall LeMaitre Vascular AnastoClip AC Closure System
  • Modèle / numéro de série
    Lot Numbers: ANC1532¿ ANC1577¿ ANC1643¿ ANC1647¿ ANC1673¿ ANC2007¿ ANC2025¿ ANC2027¿ ANC2031¿ ANC2032¿ ANC2037¿
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    US Nationwide Distribution
  • Description du dispositif
    Anastoclip AC 8cm 35 Clips (1 Each} Medium || REF # 4000-06 || The Anastoclip Clip applier consists of a rotating shaft and an integral cartridge containing titanium clips. The Anastoclip Universal Clip Remover is intended to remove Anastoclip AC Clips as necessary. It is an accessory to the Anastoclip AC Clip Applier.
  • Manufacturer
    LeMaitre Vascular, Inc.

Manufacturer

LeMaitre Vascular, Inc.
  • Adresse du fabricant
    LeMaitre Vascular, Inc., 63 2nd Ave, Burlington MA 01803-4413
  • Société-mère du fabricant (2017)
    LeMaitre Vascular, Inc.
  • Source
    USFDA