Recall of CARDIOVASCULAR PROCEDURE KIT (X-COATED PERFUSION PACK)

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by RYAN MEDICAL DISTRIBUTORS 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
    37925
  • Event Risk Class
    III
  • Event Initiated Date
    2016-07-29
  • Event Country
  • 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
    This safety alert is to notify that a portion of tubing within the terumo cardiovascular procedure kit is lablled as x-coating surface coated.However the tubing in the kit may not be coated.

Device

  • Model / Serial
    Model Catalog: 75296-01 (Lot serial: UG13); Model Catalog: 75295-01 (Lot serial: UG13); Model Catalog: 75296-01 (Lot serial: UG13T); Model Catalog: 75295-01 (Lot serial: UG20); Model Catalog: 75296-01 (Lot serial: UG20); Model Catalog: 74999-01 (Lot serial: UG20); Model Catalog: 74999-01 (Lot serial: UG20T); Model Catalog: 75295-01 (Lot serial: UG13T); Model Catalog: 75956 (Lot serial: UG20)
  • Product Description
    CArdiovasuclar procedure kit (x-coated perfusion pack);Cardiovascular procedure Kit ( x-coated heart lung);Cardiovascular procedure kit (CArdioplegia set)
  • Manufacturer

Manufacturer