Events

Recall of DALE STABILOCK 270 ENDOTRACHEAL TUBE HOLDER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by DALE MEDICAL PRODUCTS 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
    151752
  • Event Risk Class
    III
  • Event Initiated Date
    2017-04-17
  • 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
    Dale medical products inc. has identified an issue within some endotracheal tube holders (product# 270) manufactured between march and june of 2016. as a reminder these endotracheal tube holders contain the endotracheal tube holder itself along with an adhesive "faceplate" (individual product # 273). we have found that some et tube holders contain an adhesive faceplate that may lose its adhesive quality over time and therefore not perform as it should. by "over time" we mean while in storage awaiting use not after being applied.

Device

DALE STABILOCK 270 ENDOTRACHEAL TUBE HOLDER
  • Model / Serial
    Model Catalog: H84102701 (Lot serial: 06 02 16)
  • Product Description
    Endotracheal Tube Holders
  • Manufacturer
    DALE MEDICAL PRODUCTS INC.

Manufacturer

DALE MEDICAL PRODUCTS INC.