Events

Recall of STATLOCK IV PREMIUM CATHETER STABILIZATION

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BARD CANADA 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
    125183
  • Event Risk Class
    II
  • Event Initiated Date
    2017-05-11
  • 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
    Bard has identified a specific product code / lot number of statlock iv premium catheter stabilization device that may contain an incorrectly sized (shorter) retainer clip. the clip is designed to secure the spin nut of compatible iv extension sets. a shorter retainer clip would have difficulty engaging appropriately with longer infusion set luers.

Device

STATLOCK IV PREMIUM CATHETER STABILIZATION
  • Model / Serial
    Model Catalog: IV0570 (Lot serial: JUAQF675)
  • Product Description
    STATLOCK IV PREMIUM CATHETER STABILIZATION
  • Manufacturer
    BARD CANADA INC.

Manufacturer

BARD CANADA INC.