Events

Rappel de DIMENSION CLINICAL CHEMISTRY SYSTEM - IRON FLEX REAGENT CARTRIDGE

Selon Health Canada (via FOI), ce/cet/cette rappel concerne un dispositif en/au/aux/à Canada qui a été fabriqué par SIEMENS HEALTHCARE LIMITED.

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
    99319
  • Classe de risque de l'événement
    III
  • Date de mise en oeuvre de l'événement
    2016-09-02
  • 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
    Siemens healthcare diagnostics has become aware of deferoxamine interference with dimension and dimension vista iron assays at a different concentration than listed in the instructions for use (ifu). deferoxamine is listed in the dimension and dimension vista ifu's as a non-interfering substance. the concentration that was used for interference testing (250 ng/dl or 3.8 nmol/l) is significantly below what would be expected in clinical practice. siemens healthcare diagnostics is providing an update to the limitation of procedure section for the dimension and dimension vista iron assays instructions for use (ifu) to indicate that: patients treated with metal-binding drugs (e.G. deferoxamine) may have depressed iron values as chelated iron may not properly react in the iron assay.

Device

DIMENSION CLINICAL CHEMISTRY SYSTEM - IRON FLEX REAGENT CARTRIDGE
  • Modèle / numéro de série
    Model Catalog: DF85 (Lot serial: All Lots); Model Catalog: K3085 (Lot serial: All Lots)
  • Description du dispositif
    DIMENSION CLINICAL CHEMISTRY SYSTEM - IRON FLEX REAGENT CARTRIDGE;DIMENSION VISTA SYSTEM - IRON ASSAY;DIMENSION XPAND SYSTEM - IRON (IRON) ASSAY;DIMENSION EXL SYSTEM - IRON (IRON) ASSAY
  • Manufacturer
    SIEMENS HEALTHCARE LIMITED

Manufacturer

SIEMENS HEALTHCARE LIMITED
  • Adresse du fabricant
    OAKVILLE
  • Société-mère du fabricant (2017)
    Siemens Ag
  • Source
    HC