Recall of STRYKER MEDICAL BEDS

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
    71323
  • Event Risk Class
    III
  • Event Initiated Date
    2012-03-27
  • 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 medical has determined that units manufactured from september 1 2004 through november 30 2007 did not receive updated preventive maintenance information.

Device

  • Model / Serial
    Model Catalog: 2040000000 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 3002CUSTOM (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 2030 EPIC (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 2030 EPIC+ (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 3002000000 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 3002001201 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 3002 ZOOM (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 2030000000 (Lot serial: >10 NUMBERS CONTACT MFG)
  • Product Description
    STRYKER MEDICAL BED BRAKE PLATE
  • Manufacturer

Manufacturer

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