Events

Recall of FILLING TUBE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by LIEBEL-FLARSHEIM COMPANY LLC.

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
    101358
  • Event Risk Class
    II
  • Event Initiated Date
    2010-02-03
  • 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
    The manufacturer received reports of sterilized packages of handi-fil disposable syringe fill tube that are unsealed. (catalogue number 302050 lot number 7159027).

Device

FILLING TUBE
  • Model / Serial
    Model Catalog: 302050 (Lot serial: 7159027)
  • Product Description
    HANDI-FIL DISPOSABLE SYRINGE FILL TUBE
  • Manufacturer
    LIEBEL-FLARSHEIM COMPANY LLC

Manufacturer

LIEBEL-FLARSHEIM COMPANY LLC
  • Manufacturer Address
    CINCINNATI
  • Manufacturer Parent Company (2017)
    Guerbet
  • Source
    HC