Events

Recall of ACCU-CHEK AVIVA 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
    33112
  • Event Risk Class
    II
  • Event Initiated Date
    2005-11-08
  • 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
    Potential corruption of the meter's flash memory caused by a flipped bit. the manifested malfunctions of the flipped bit were a complete shutdown of the meter or a too-low and non-plausible result.

Device

ACCU-CHEK AVIVA METER
  • Model / Serial
    Model Catalog: 03532313001 (Lot serial: SERIAL # BELOW 526 10 999 999)
  • Product Description
    ACCU-CHEK AVIVA METER
  • Manufacturer
    ROCHE DIAGNOSTICS

Manufacturer

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