Events

Recall of MEDICINA ENTERAL FEEDING PUMP

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by MCARTHUR MEDICAL SALES INC..

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
    146702
  • Event Risk Class
    III
  • Event Initiated Date
    2016-02-15
  • 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 safety and performance of these devices has not been properly evaluated and so the ce marking of the devices is not valid. medicina therefore advises that the product is recalled from the market. the p700 and p900 pumps have previously been recalled however it is possible that not all of these devices have been returned and medicina requests that any devices with model numbers p500 p700 and p900 be returned to them.

Device

MEDICINA ENTERAL FEEDING PUMP
  • Model / Serial
    Model Catalog: P900 (Lot serial: 12030331); Model Catalog: P900 (Lot serial: 12080008); Model Catalog: P900 (Lot serial: 12030341)
  • Product Description
    MEDICINA ENTERAL FEEDING PUMPS
  • Manufacturer
    MCARTHUR MEDICAL SALES INC.

Manufacturer

MCARTHUR MEDICAL SALES INC.