Events

Recall of DIMENSION VISTA SYSTEM - DRUG CALIBRATOR

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SIEMENS HEALTHCARE LIMITED.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    27465
  • Event Risk Class
    II
  • Event Initiated Date
    2013-02-22
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    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.
  • Extra notes in the data
  • Reason
    Siemens has confirmed complaints of low qc and patient recovery with the dimension vista loci digoxin (digxn) flex reagent cartridge when calibrating digxn with either drug 4 cal (kc460) lot 2kd052 or drug 4 cal (kc460a) lot 2kd053. internal testing has shown an average 15% low bias in the therapeutic range of 0.9 to 2.0 ng/ml.

Device

DIMENSION VISTA SYSTEM - DRUG CALIBRATOR
  • Model / Serial
    Model Catalog: KC460 (Lot serial: 2KD052); Model Catalog: KC460A (Lot serial: 2KD052); Model Catalog: KC460 (Lot serial: 2KD053); Model Catalog: KC460A (Lot serial: 2KD053)
  • Product Description
    DIMENSION VISTA DRUG 4 CALIBRATOR
  • Manufacturer
    SIEMENS HEALTHCARE LIMITED

Manufacturer

SIEMENS HEALTHCARE LIMITED
  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC