Events

Recall of PLUM XL 3 MULTI-LINE INFUSION SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by ABBOTT LABORATORIES DIAGNOSTIC DIVISION.

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
    25708
  • Event Risk Class
    II
  • 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
    Upgrade software in order to restore pump settings at the last ordely shutdown when there is a non-ordely shutdown(ex: dead battery power failure).

Device

PLUM XL 3 MULTI-LINE INFUSION SYSTEM

Manufacturer

ABBOTT LABORATORIES DIAGNOSTIC DIVISION
  • Manufacturer Address
    ABBOTT PARK
  • Source
    HC