Events

Recall of COBAS INTEGRA SYSTEM - AMMONIA

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

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
    22589
  • Event Risk Class
    II
  • Event Initiated Date
    2000-02-11
  • 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
    Plasma collected with lithium heparin may give erratic and unpredictable results when compared to edta plasma when using the integra ammmonia reagent on the cobas integra 400 and 700 analyserx.

Device

COBAS INTEGRA SYSTEM - AMMONIA
  • Model / Serial
    Model Catalog: 0766682 (Lot serial: all lot numbers.)
  • Product Description
    cat.# 0766682
  • Manufacturer
    ROCHE DIAGNOSTICS

Manufacturer

ROCHE DIAGNOSTICS
  • Manufacturer Address
    LAVAL
  • Manufacturer Parent Company (2017)
    Roche Holding AG
  • Source
    HC