Events

Recall of URETHRAL PROCEDURAL TRAY WITH SYRINGE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by TELEFLEX MEDICAL 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
    73922
  • Event Risk Class
    II
  • Event Initiated Date
    2011-04-07
  • 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
    This recall supersedes teleflex's march 4 2011 communication. teleflex medical is withdrawing the rusch irrigation trays catalogue number 67890 and 68895 from the market. these trays contain alcohol prep pads recalled by triad due to concern about bacterial contamination and . all trays containing the alcohol prep pads recalled by triad should be returned to teleflex medical.

Device

URETHRAL PROCEDURAL TRAY WITH SYRINGE
  • Model / Serial
    Model Catalog: 67890 (Lot serial: >10 numbers contact mfg); Model Catalog: 68895 (Lot serial: >10 numbers contact mfg)
  • Product Description
    Urethral Procedure Tray With Syringe
  • Manufacturer
    TELEFLEX MEDICAL CANADA INC.

Manufacturer

TELEFLEX MEDICAL CANADA INC.