Events

Recall of CODE BLUE ADULT RESUSCITATORS

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by TRUDELL MEDICAL MARKETING 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
    89495
  • Event Risk Class
    II
  • Event Initiated Date
    2002-08-13
  • 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
    Disk seal at rear of bag may not be seated allowing air oxygen to exit.

Device

CODE BLUE ADULT RESUSCITATORS
  • Model / Serial
    Model Catalog: 7500 (Lot serial: 001 through 365 and those); Model Catalog: 7500 (Lot serial: beginning with F H); Model Catalog: 7500 (Lot serial: 001 through 106); Model Catalog: 7500 (Lot serial: all lots beginning with D E)
  • Product Description
    ressucitator code blue
  • Manufacturer
    TRUDELL MEDICAL MARKETING LIMITED

Manufacturer

TRUDELL MEDICAL MARKETING LIMITED