Recall of SDC HD CAPTURE RECORDER W/PRINTER

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
    50937
  • Event Risk Class
    II
  • Event Initiated Date
    2009-11-04
  • 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
    Stryker endoscopy was aware that the sdc hd picture/video capture device would not be able to assign the correct time/date stamp for saved files after december 31st 2009. on january 1st 2010 the system date for all sdc hd units would re-start from october 1st 2001 and begin incrementing from that point onwards. this event would not affect how pictures or videos were captured using sdc hd during surgery however the system date would be incorrect and users would not be able to correct this issue without a software upgrade.

Device

  • Model / Serial
    Model Catalog: 240-050-890 (Lot serial: ALL LOT NUMBERS); Model Catalog: 240-050-888 (Lot serial: ALL LOT NUMBERS)
  • Product Description
    SDC HD Capture Device
  • Manufacturer

Manufacturer

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