Recall of ENS. POUR ADENO-AMYGDALECTOMIE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by CARDINAL HEALTH CANADA INC..

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
    61069
  • Event Risk Class
    I
  • Event Initiated Date
    2014-08-06
  • 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
    Baxter that they have initiated a recall of various lots of buretrol solution sets (component 2c7564-buretrol solution set with 150ml interlink burette) which are found in the presource kit. this action has been initiated due to complaints for separation between the burette chamber and the drip chamber.

Device

  • Model / Serial
    Model Catalog: PE30TA'XXX' (Lot serial: 197533); Model Catalog: PE30TAHRA (Lot serial: 197533); Model Catalog: PE30TAHRA (Lot serial: 166213); Model Catalog: PE30TA'XXX' (Lot serial: 166213); Model Catalog: PE30TAHRA (Lot serial: 163038); Model Catalog: PE30TA'XXX' (Lot serial: 163038)
  • Product Description
    PRESOURCE KIT PE30TAHRA (KIT TONSILS AND ADENOIDS)
  • Manufacturer

Manufacturer

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