Events

Recall of WALLACE OOCYTE RECOVERY SET

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SMITHS MEDICAL INTERNATIONAL LTD..

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
    28372
  • Event Risk Class
    III
  • Event Initiated Date
    2005-11-29
  • 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 needle used on some lots may be blocked in the region of the hub.

Device

WALLACE OOCYTE RECOVERY SET
  • Model / Serial
    Model Catalog: (Lot serial: 479366); Model Catalog: (Lot serial: 482974)
  • Product Description
    WALLACE OOCYTE RECOVERY SET
  • Manufacturer
    SMITHS MEDICAL INTERNATIONAL LTD.

Manufacturer

SMITHS MEDICAL INTERNATIONAL LTD.
  • Manufacturer Address
    HYTHE
  • Manufacturer Parent Company (2017)
    Smiths Group Plc
  • Source
    HC