Events

Recall of ACCU-CHEK INFORM II + RF METER

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
    140416
  • Event Risk Class
    II
  • Event Initiated Date
    2013-02-25
  • 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
    This recall is related to possible erroneous decoding of ean 13 barcodes used for operator and/or patient identification under specific conditions observed on the systems accu-chek inform ii meters and coaguchek xs pro monitors.

Device

ACCU-CHEK INFORM II + RF METER
  • Model / Serial
    Model Catalog: 05060303001 (Lot serial: ALL LOTS); Model Catalog: 05060311001 (Lot serial: ALL LOTS); Model Catalog: 05530199190 (Lot serial: ALL LOTS)
  • Product Description
    Accu-Chek Inform II + RF Meter
  • Manufacturer
    ROCHE DIAGNOSTICS

Manufacturer

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