Events

Recall of BLOOD PACK UNIT WITH CPD

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BAXTER CORPORATION.

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
    25586
  • Event Risk Class
    III
  • Event Initiated Date
    2007-05-01
  • 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
    Manufacturer has received complaints of various amounts of anticoagulant in between the donor needle and the sampling pouch.

Device

BLOOD PACK UNIT WITH CPD
  • Model / Serial
    Model Catalog: CGR8496B (Lot serial: ALL LOT NUMBERS); Model Catalog: CGR8448B (Lot serial: ALL LOT NUMBERS)
  • Product Description
    BLOOD PACK UNIT WITH CPD
  • Manufacturer
    BAXTER CORPORATION

Manufacturer

BAXTER CORPORATION