Recall of BEHRING NEPHELOMETER SYSTEM - N LATEX IGE

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
    130383
  • Event Risk Class
    III
  • Event Initiated Date
    2014-06-16
  • 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
    Siemens healthcare diagnostics has confirmed an increase in the rate of technical flags with the n latex ige mono reagent lots mentioned above. the errors can occur on calibration qc and/or patient sample. no result is given with the technical flag. in such cases a calibration curve cannot be established. in rare cases invalid qc results might be observed leading to invalid runs.

Device

  • Model / Serial
    Model Catalog: OQTG15 (Lot serial: 169658C); Model Catalog: OQTG15 (Lot serial: 169658B); Model Catalog: OQTG15 (Lot serial: 169658A); Model Catalog: OQTG15 (Lot serial: 169658)
  • Product Description
    BEHRING NEPHELOMETER SYSTEM - N LATEX IGE
  • Manufacturer

Manufacturer

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