Safety Alert for Zurpaz Steerable Sheath 8.5F Asymmetric and Symmetric Curves

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Creganna Tactx Medical.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2017-06-05
  • Event Date Posted
    2017-06-05
  • Event Country
  • Event Source
    DH
  • Event Source URL
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: creganna tactx medical zurpaz steerable sheath 8.5f asymmetric and symmetric curves boston scientific has issued a medical device safety alert concerning zurpaz steerable sheath, 8.5f asymmetric and symmetric curves, manufactured by creganna tactx medical. the affected products are identified as follows: 8.5f asymmetric curve (us model) material number: m004usmca85200; lot number: 364951; expiration date: 13-dec-2018 8.5f symmetric curve (us model) material number: m004usmc85100; lot number: 383271; expiration date: 3-jan-2019 boston scientific, a distributor of the zurpaz steerable sheath, became aware from the manufacturer, creganna medical (also doing business as creganna tactx medical), that a blister near the pouch seal may result in a compromised sterile barrier. pouch blistering might not be obvious to the user. if it is identified, the device can be readily exchanged resulting in an insignificant prolongation in procedure. if the sterile barrier was compromised and the device was used, the most severe expected harm is a potential infection; however no reports of patient harm have been received. further distribution or use of the affected product should cease immediately. affected users should segregate the product immediately and return it to boston scientific. product recall is on-going. according to the local supplier, the affected products are not distributed in hong kong if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 5 june 2017.

Device

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Creganna Tactx Medical Zurpaz Steerable Sheath 8.5F Asymmetric and Symmetric Curves
  • Manufacturer

Manufacturer