Recall of DIMENSION EXL SYSTEM - (TROPONIN) TNI ASSAY

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
    137178
  • Event Risk Class
    III
  • Event Initiated Date
    2011-09-02
  • Event Country
  • 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
    Internal testing has confirmed low recovery of qc and patient samples. use of one of these lots may show a downward shift in qc and patient results. this decrease may cause a sample that is slightly above the 99th percentile (0.056 ng/ml) of a reference population to read below this value. at higher values of tni samples will remain positive and the bias is not clinically significant.

Device

  • Model / Serial
    Model Catalog: RF621 (Lot serial: EA2111); Model Catalog: RF621 (Lot serial: FB2134); Model Catalog: RF621 (Lot serial: ED2147); Model Catalog: RF621 (Lot serial: ED2098)
  • Product Description
    DIMESION EXL SYSTEM-(TROPONIN) TNI ASSAY
  • Manufacturer

Manufacturer

  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
  • Source
    HC