Events

Recall of STRYKER ADEL MATERNITY BED

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by STRYKER MEDICAL QUEBEC LP.

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
    150210
  • Event Risk Class
    II
  • Event Initiated Date
    2004-04-19
  • 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
    A potential shock hazard exists if the nightlight is damaged.

Device

STRYKER ADEL MATERNITY BED
  • Model / Serial
    Model Catalog: (Lot serial: 5010-000-000); Model Catalog: (Lot serial: 5012-000-000); Model Catalog: (Lot serial: 4700-000-000)
  • Product Description
    4700-5010-5012 BIRTHING BEDS
  • Manufacturer
    STRYKER MEDICAL QUEBEC LP

Manufacturer

STRYKER MEDICAL QUEBEC LP
  • Manufacturer Address
    L'ISLET
  • Source
    HC