Recall of 3CC LUER-LOK TIP SYRINGE * NEEDLE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BECTON DICKINSON 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
    82127
  • Event Risk Class
    II
  • Event Initiated Date
    2016-09-19
  • Event Country
  • 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
    Bd is conducting a voluntary product recall of several bd catalogues of luer-lok syringes and luer-lok syringe with precisionglide needle since the sterility of the product cannot be assured. this may result in increased risk of infection. no adverse event has been reported for this issue at this time. bd is actively working on implementing corrective actions to address this issue.

Device

  • Model / Serial
    Model Catalog: 309571 (Lot serial: 6117580); Model Catalog: 309657 (Lot serial: 6113717); Model Catalog: 309604 (Lot serial: 6113717); Model Catalog: 309604 (Lot serial: 6117889); Model Catalog: 309604 (Lot serial: 6117891); Model Catalog: 309657 (Lot serial: 6117889); Model Catalog: 309657 (Lot serial: 6117891)
  • Product Description
    3ml Syringe Luer-Lok Tip with PrecisionGlide Needle;10 ml & 3ml Syringe Luer-Lok Tip
  • Manufacturer

Manufacturer