Events

Rappel de ARROW-HOWES MULTI-LUMEN CENTRAL VENOUS CATHETERIZATION SET

Selon Health Canada (via FOI), ce/cet/cette rappel concerne un dispositif en/au/aux/à Canada qui a été fabriqué par TELEFLEX MEDICAL CANADA 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
    46208
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2017-11-29
  • Pays de l'événement
    Canada
  • Source de l'événement
    HC
  • Notes / Alertes
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • Notes supplémentaires dans les données
  • Cause
    Arrow international is recalling the referenced products because some of the products may be missing a sticker that contains the lot number expiration date and unique device identification (udi) information.

Device

ARROW-HOWES MULTI-LUMEN CENTRAL VENOUS CATHETERIZATION SET
  • Modèle / numéro de série
    Model Catalog: ASK15703-PRJ (Lot serial: 13F17D0112); Model Catalog: ASK-12703-PRJ (Lot serial: 13F17D0112); Model Catalog: ASK15703-PRJ (Lot serial: 13F17B0279); Model Catalog: ASK-12703-PRJ (Lot serial: 13F17B0279); Model Catalog: ASK15703-PRJ (Lot serial: 13F17B0265); Model Catalog: ASK-12703-PRJ (Lot serial: 13F17B0265); Model Catalog: CDA-21242-1A (Lot serial: 13F17H0503); Model Catalog: CDA-21242-1A (Lot serial: 13F16L0209); Model Catalog: CDA-21242-1A (Lot serial: 13F17F0437); Model Catalog: CDA-47702-P1A (Lot serial: 13F17H0566); Model Catalog: CDA-45703-P1A (Lot serial: 13F17H0566); Model Catalog: CDA-42802-P1A (Lot serial: 13F17H0566); Model Catalog: CDA-42703-P1A (Lot serial: 13F17H0566); Model Catalog: CA-45703-P1A (Lot serial: 13F17H0566); Model Catalog: CA-42703-P1A (Lot serial: 13F17H0566); Model Catalog: CDA-47702-P1A (Lot serial: 13F17G0541); Model Catalog: CDA-45703-P1A (Lot serial: 13F17G0541); Model Catalog: CDA-42802-P1A (Lot serial: 13F17G0541); Model Catalog: CDA-42703-P1A (Lot serial:
  • Description du dispositif
    CENTRAL VENOUS CATHETERIZATION KITS/SETS;TWO-LUMEN CENTRAL VENOUS ACCESS KIT;AGB+ PRESSURE INJECTABLE MULTI-LUMEN CVC KIT;PERCUTANEOUS SHEATH INTRODUCER SET;ARROWG+ARD BLUE PLUS CENTRAL VENOUS CATHETER KITS;ARROWG+ARD BLUE PLUS CENTRAL VENOUS CATHETER KIT
  • Manufacturer
    TELEFLEX MEDICAL CANADA INC.

Manufacturer

TELEFLEX MEDICAL CANADA INC.