Events

Recall of CVP CATHETER 3-LUMEN EXPANDED KIT

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
    97808
  • Event Risk Class
    II
  • Event Initiated Date
    2000-03-31
  • 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
    Microbial contamination confirmed.

Device

CVP CATHETER 3-LUMEN EXPANDED KIT
  • Model / Serial
    Model Catalog: 41401 (Lot serial: 8SN 43030SN); Model Catalog: 41401 (Lot serial: 46387SN 50562SN//); Model Catalog: 41401 (Lot serial: ref.41401: 4118SN 43030SN)
  • Product Description
    CLINIPAD POVISONE-IODINE RECALL
  • Manufacturer
    ABBOTT LABORATORIES DIAGNOSTIC DIVISION

Manufacturer

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