Events

Recall of STRYKER 40L HIGH FLOW INSUFFLATOR - TUBING

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

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
    144348
  • Event Risk Class
    II
  • Event Initiated Date
    2010-03-23
  • 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
    Stryker endoscopy has become aware that the stryker heated insufflators may have been received with no expiration date printed on the label. additionally it was discovered that no packaging shelf-life testing had been completed for those products during the initial product launch. stryker has also become aware that the above referenced products may have been released for distribution and sold in countries that may have regulations regarding label expiration.

Device

STRYKER 40L HIGH FLOW INSUFFLATOR - TUBING
  • Model / Serial
    Model Catalog: 0620-030-407 (Lot serial: >100 NUMBERSCONTACT MFG)
  • Product Description
    STRYKER HEATED INSUFFLATORS
  • Manufacturer
    STRYKER CANADA LP

Manufacturer

STRYKER CANADA LP
  • Manufacturer Address
    HAMILTON
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    HC