Events

Recall of HOMECHOICE AUTOMATED PD SYSTEM - CASSETTES

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
    106676
  • Event Risk Class
    II
  • Event Initiated Date
    1996-07-02
  • 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

Device

HOMECHOICE AUTOMATED PD SYSTEM - CASSETTES
  • Model / Serial
    Model Catalog: (Lot serial: H95L1259X H95C0660X); Model Catalog: (Lot serial: H95C0658X-C95L1258X H95C0659X); Model Catalog: (Lot serial: H95xxxxxx H95Axxxxxx); Model Catalog: (Lot serial: H95L1260X); Model Catalog: (Lot serial: LOTS BEGINNING WITH 1260X); Model Catalog: (Lot serial: H95Bxxxxx H95C01xxx-H95C05xxx)
  • Manufacturer
    BAXTER CORPORATION

Manufacturer

BAXTER CORPORATION