Events

Recall of ADVANCED PERFUSION SYSTEM 1 - BASE UNIT

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by RYAN MEDICAL DISTRIBUTORS 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
    23263
  • Event Risk Class
    III
  • Event Initiated Date
    2012-07-10
  • 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
    Some users operating a terumo advanced perfusion system 1 with a modified cable to connect the system to an occluder for the sarns modular perfusion system 8000. the cable is not specified for use with terumo system 1 and its use in this manner constitutes an off label use.

Device

ADVANCED PERFUSION SYSTEM 1 - BASE UNIT
  • Model / Serial
    Model Catalog: 801763 (Lot serial: 0011-1443)
  • Product Description
    ADVANCED PERFUSION SYSTEM 1 - BASE UNIT
  • Manufacturer
    RYAN MEDICAL DISTRIBUTORS INC.

Manufacturer

RYAN MEDICAL DISTRIBUTORS INC.