Events

Recall of COMBI SLING DELUXE CHILD

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

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
    64649
  • Event Risk Class
    II
  • Event Initiated Date
    2009-04-08
  • 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 premature failure of the stitching at the junction of the shoulder strap and the sling body can lead to the detachment of the shoulder strap resulting in possible patient fall.

Device

COMBI SLING DELUXE CHILD
  • Model / Serial
    Model Catalog: 626002C (Lot serial: ); Model Catalog: 626003X (Lot serial: ); Model Catalog: 626002 (Lot serial: ); Model Catalog: 626003 (Lot serial: ); Model Catalog: 626002C-M (Lot serial: ); Model Catalog: 626002M (Lot serial: ); Model Catalog: 626003M (Lot serial: )
  • Product Description
    Combi Sling Deluxe Child
  • Manufacturer
    ARJOHUNTLEIGH MAGOG

Manufacturer

ARJOHUNTLEIGH MAGOG
  • Manufacturer Address
    MAGOG
  • Manufacturer Parent Company (2017)
    Getinge AB
  • Source
    HC