Events

Recall of KIMVENT*MICROCUFF* SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE ORAL MURPHY EYE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by CANADIAN HOSPITAL SPECIALTIES LTD..

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
    85846
  • Event Risk Class
    I
  • Event Initiated Date
    2014-11-21
  • 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
    It was identified that the inflation line may detach from the endotracheal tubes during use.

Device

KIMVENT*MICROCUFF* SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE ORAL MURPHY EYE
  • Model / Serial
    Model Catalog: 13222 (Lot serial: AA4111V02); Model Catalog: 13221 (Lot serial: AA4111V02); Model Catalog: 13222 (Lot serial: AA4134V02); Model Catalog: 13221 (Lot serial: AA4134V02); Model Catalog: 13222 (Lot serial: AA4097V01); Model Catalog: 13221 (Lot serial: AA4097V01)
  • Product Classification
    Anesthesiology Devices
  • Product Description
    KimVent Microcuff Subglottic Suctioning Endotracheal Tube
  • Manufacturer
    CANADIAN HOSPITAL SPECIALTIES LTD.

Manufacturer

CANADIAN HOSPITAL SPECIALTIES LTD.